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"apellidos" => "Chang" ] ] ] ] ] "idiomaDefecto" => "es" "Traduccion" => array:1 [ "en" => array:9 [ "pii" => "S1578219013002655" "doi" => "10.1016/j.adengl.2012.06.032" "estado" => "S300" "subdocumento" => "" "abierto" => array:3 [ "ES" => true "ES2" => true "LATM" => true ] "gratuito" => true "lecturas" => array:1 [ "total" => 0 ] "idiomaDefecto" => "en" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S1578219013002655?idApp=UINPBA000044" ] ] "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S0001731012004176?idApp=UINPBA000044" "url" => "/00017310/0000010500000001/v1_201401250106/S0001731012004176/v1_201401250106/es/main.assets" ] ] "itemSiguiente" => array:19 [ "pii" => "S1578219013002667" "issn" => "15782190" "doi" => "10.1016/j.adengl.2012.09.025" "estado" => "S300" "fechaPublicacion" => "2014-01-01" "aid" => "734" "copyright" => "Elsevier España, S.L. and AEDV" "documento" => "article" "crossmark" => 0 "subdocumento" => "ssu" "cita" => "Actas Dermosifiliogr. 2014;105:18-30" "abierto" => array:3 [ "ES" => true "ES2" => true "LATM" => true ] "gratuito" => true "lecturas" => array:2 [ "total" => 10807 "formatos" => array:3 [ "EPUB" => 41 "HTML" => 7995 "PDF" => 2771 ] ] "en" => array:13 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Review</span>" "titulo" => "Drug-Induced Lupus Erythematosus" "tienePdf" => "en" "tieneTextoCompleto" => "en" "tieneResumen" => array:2 [ 0 => "en" 1 => "es" ] "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "18" "paginaFinal" => "30" ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Lupus eritematoso inducido por fármacos" ] ] "contieneResumen" => array:2 [ "en" => true "es" => true ] "contieneTextoCompleto" => array:1 [ "en" => true ] "contienePdf" => array:1 [ "en" => true ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:7 [ "identificador" => "fig0015" "etiqueta" => "Figure 3" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr3.jpeg" "Alto" => 587 "Ancho" => 900 "Tamanyo" => 76790 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">A 79-year-old woman with a history of metastatic ovarian cancer. The back lesions are clinically and histopathologically compatible with subacute lupus erythematosus of 2 months’ duration. The patient reported having taken bisoprolol in recent months, and the lesions resolved after the drug was stopped.</p>" ] ] ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "M. Pretel, L. Marquès, A. España" "autores" => array:3 [ 0 => array:2 [ "nombre" => "M." "apellidos" => "Pretel" ] 1 => array:2 [ "nombre" => "L." "apellidos" => "Marquès" ] 2 => array:2 [ "nombre" => "A." "apellidos" => "España" ] ] ] ] ] "idiomaDefecto" => "en" "Traduccion" => array:1 [ "es" => array:9 [ "pii" => "S0001731012004516" "doi" => "10.1016/j.ad.2012.09.007" "estado" => "S300" "subdocumento" => "" "abierto" => array:3 [ "ES" => true "ES2" => true "LATM" => true ] "gratuito" => true "lecturas" => array:1 [ "total" => 0 ] "idiomaDefecto" => "es" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S0001731012004516?idApp=UINPBA000044" ] ] "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S1578219013002667?idApp=UINPBA000044" "url" => "/15782190/0000010500000001/v1_201401220123/S1578219013002667/v1_201401220123/en/main.assets" ] "itemAnterior" => array:19 [ "pii" => "S1578219013002643" "issn" => "15782190" "doi" => "10.1016/j.adengl.2013.07.001" "estado" => "S300" "fechaPublicacion" => "2014-01-01" "aid" => "876" "copyright" => "Elsevier España, S.L. and AEDV" "documento" => "article" "crossmark" => 0 "subdocumento" => "sco" "cita" => "Actas Dermosifiliogr. 2014;105:1-4" "abierto" => array:3 [ "ES" => true "ES2" => true "LATM" => true ] "gratuito" => true "lecturas" => array:2 [ "total" => 3452 "formatos" => array:3 [ "EPUB" => 47 "HTML" => 2527 "PDF" => 878 ] ] "en" => array:11 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Opinion article</span>" "titulo" => "Clinical Significance of Immunogenicity in Biologic Therapy" "tienePdf" => "en" "tieneTextoCompleto" => "en" "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "1" "paginaFinal" => "4" ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Relevancia clínica de la inmunogenicidad en las terapias biológicas" ] ] "contieneTextoCompleto" => array:1 [ "en" => true ] "contienePdf" => array:1 [ "en" => true ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:7 [ "identificador" => "fig0005" "etiqueta" => "Figure 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 1693 "Ancho" => 2337 "Tamanyo" => 215413 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Algorithm for decision making in patients who do not respond to anti-TNF treatment introducing the concept of primary and secondary failure depending on factors related to immunogenicity. 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"apellidos" => "Vásquez" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">b</span>" "identificador" => "aff0010" ] ] ] 4 => array:3 [ "nombre" => "R." "apellidos" => "Fernández" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">b</span>" "identificador" => "aff0010" ] ] ] 5 => array:3 [ "nombre" => "P." "apellidos" => "Chang" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">c</span>" "identificador" => "aff0015" ] ] ] ] "afiliaciones" => array:3 [ 0 => array:3 [ "entidad" => "Servicio de Dermatología, CHUVI y Universidad de Vigo, Vigo, Spain" "etiqueta" => "a" "identificador" => "aff0005" ] 1 => array:3 [ "entidad" => "Sección de Micología, Hospital General Dr. Manuel Gea González, México DF, Mexico" "etiqueta" => "b" "identificador" => "aff0010" ] 2 => array:3 [ "entidad" => "Hospital General de Enfermedades, Instituto Guatemalteco de Seguridad Social, Ciudad de Guatemala, Guatemala" "etiqueta" => "c" "identificador" => "aff0015" ] ] "correspondencia" => array:1 [ 0 => array:3 [ "identificador" => "cor0005" "etiqueta" => "⁎" "correspondencia" => "Corresponding author." ] ] ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Micosis sistémicas en pacientes con virus de la inmunodeficiencia humana/sida" ] ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:7 [ "identificador" => "fig0070" "etiqueta" => "Figure 14" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr14.jpeg" "Alto" => 669 "Ancho" => 900 "Tamanyo" => 94194 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0110" class="elsevierStyleSimplePara elsevierViewall">Crusted lesions and umbilicated lesions (different phases of development) caused by <span class="elsevierStyleItalic">Histoplasma capsulatum</span> in a patient with immune reconstitution inflammatory syndrome in different phases of development.</p>" ] ] ] "textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Introduction</span><p id="par0005" class="elsevierStylePara elsevierViewall">Systemic mycoses can be classified according to whether the causative agent is a systemic fungal pathogen (<span class="elsevierStyleItalic">Blastomyces dermatitidis, Coccidioides immitis, Histoplasma capsulatum</span> [variants <span class="elsevierStyleItalic">capsulati</span> and <span class="elsevierStyleItalic">duboisii</span>], and <span class="elsevierStyleItalic">Paracoccidioides brasiliensis</span>) or one of an increasing number of opportunistic fungal pathogens normally found in the environment. These fungi are thermally dimorphic microorganisms with 2 phases. Transition from the mycelial to yeast phase is normally associated with a change in temperature from 25<span class="elsevierStyleHsp" style=""></span>°C to 37<span class="elsevierStyleHsp" style=""></span>°C. With the exception of <span class="elsevierStyleItalic">C immitis</span>, which forms spherules with endospores, the natural phase of each of these fungi is a mold, while the histic form is a yeast.<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1–4</span></a></p><p id="par0010" class="elsevierStylePara elsevierViewall">All these fungi are essentially pulmonary pathogens and inhalation of conidia is the most likely route of entry to the respiratory tract. Skin manifestations generally require disseminated infection but can occasionally be due to traumatic implantation of material contaminated with the fungi. The majority of deep-seated mycoses usually occur in certain regions of North America, South America, Central America, and Africa. These infections and their corresponding skin manifestations have become the most frequent opportunistic infection among the increasingly large populations of individuals with severe immune deficiencies, including AIDS. Skin manifestations are important for 2 reasons. First, they may preempt other clinical manifestations, including pulmonary or neurologic conditions, and so their detection can enable early treatment. Second, a skin biopsy can be readily taken with minimally invasive procedures. The biopsy samples enable microbiological culture and histopathologic study, which are sometimes necessary for correct diagnosis. The diagnostic yield for such procedures is high. The present article should therefore be useful for younger dermatologists and for all those interested in the study of mycosis. We have focused on 3 types of infection—histoplasmosis, coccidioidomycosis, and cryptococcosis—as these are the most prevalent. They are also the infections for which we have most information and experience.</p><p id="par0015" class="elsevierStylePara elsevierViewall">We have conducted a thorough review of the literature on epidemiologic, clinical, diagnostic, and therapeutic information pertaining to endemic systemic mycoses (histoplasmosis, coccidioidomycosis, and cryptococcosis) in adult patients infected with the human immunodeficiency virus (HIV)/AIDS, from the first reports of cases until the end of 2011. We have also included data and images from our own experience.</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Histoplasmosis</span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Etiology</span><p id="par0020" class="elsevierStylePara elsevierViewall">Histoplasmosis is caused by the dimorphic fungus <span class="elsevierStyleItalic">H capsulatum</span>, which has 2 variants that are pathogenic for humans, the <span class="elsevierStyleItalic">duboisii</span> variant, found mainly in Africa, and the <span class="elsevierStyleItalic">capsulatum</span> variant, found mainly in North and South America. The disease can, however, occur throughout the world.<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a> The fungus is present in the excrement of bats and certain birds, and can remain in the environment for prolonged periods.</p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0040">Transmission Mechanism</span><p id="par0025" class="elsevierStylePara elsevierViewall">Infection is acquired by inhalation of the mycelial form and primarily affects the lungs. Spontaneous resolution occurs in 95% of the patients, and infection induces immunologic memory.<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">6</span></a> The pathogenic process after inhalation of conidia initially involves localized pneumonitis, followed by hematogenous spread after 2 weeks, and cell-mediated immune response after 3 weeks. In patients with AIDS, infection can progress or become reactivated when CD4 levels decrease.<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">7</span></a></p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0045">Epidemiology</span><p id="par0030" class="elsevierStylePara elsevierViewall">Histoplasmosis has been accepted as one of the defining diseases of AIDS since 1987. However, with the introduction of antiretroviral therapy (ART), CD4<span class="elsevierStyleSup">+</span> levels have come under better control with a decline in the incidence of fungal infections 20% to 25% below the incidences in the 1990s.<a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">8–11</span></a></p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0050">Overview of Symptoms</span><p id="par0035" class="elsevierStylePara elsevierViewall">The symptoms of acute pulmonary histoplasmosis include fever, general malaise, weight loss, cough, and chest pain. Infection can follow a rapid course with involvement of the reticuloendothelial system, in which case it is almost always fatal. Central nervous system (CNS) involvement can be primary or it may be associated with disseminated disease (5% to 10% of cases). Manifestations include meningitis, encephalitis, and vascular syndromes.<a class="elsevierStyleCrossRefs" href="#bib0035"><span class="elsevierStyleSup">7,12</span></a> Half the patients with disseminated forms have impaired adrenal function, but only 7% actually present with adrenal insufficiency. Ocular damage in the form of panophthalmitis and uveitis may occur. Ocular histoplasmosis syndrome has been reported after uveitis or choroiditis; in most cases (90%), these processes are unilateral.<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">13</span></a></p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0055">Skin Manifestations</span><p id="par0040" class="elsevierStylePara elsevierViewall">Primary skin lesions are uncommon. Skin involvement occurs in association with disseminated histoplasmosis in 70% to 80% of cases (<a class="elsevierStyleCrossRefs" href="#fig0005">Figs. 1–3</a>). Skin manifestations are observed mainly in adults and more frequently in South America, where the strains are thought to be more virulent. There are no specific skin lesions. Two-thirds of patients experience mucosal involvement, particularly in the oropharyngeal region (<a class="elsevierStyleCrossRef" href="#fig0020">Fig. 4</a>). Erythema nodosum or polymorphous erythema may also be present in association with pulmonary histoplasmosis.<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">12</span></a></p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><elsevierMultimedia ident="fig0010"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia><elsevierMultimedia ident="fig0020"></elsevierMultimedia></span><span id="sec0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0060">Laboratory Tests and Imaging</span><p id="par0045" class="elsevierStylePara elsevierViewall">Laboratory observations used to support diagnosis of histoplasmosis include anemia, leukopenia, thrombocytopenia, abnormal liver enzymes, and elevated lactate dehydrogenase and ferritin.</p><p id="par0050" class="elsevierStylePara elsevierViewall">A smear with May-Grünwald-Giemsa or periodic acid-Schiff (PAS) stains can be obtained from lesions, bone marrow samples, sputum samples, or material obtained from bronchoscopy to visualize the yeasts (<a class="elsevierStyleCrossRef" href="#fig0025">Fig. 5</a>).<a class="elsevierStyleCrossRef" href="#bib0070"><span class="elsevierStyleSup">14</span></a> Intradermal reaction is not very useful in patients with AIDS. Although histopathologic study with PAS, Giemsa, or Gomori-Grocott stains is very helpful, culture is still the gold standard for diagnosis.</p><elsevierMultimedia ident="fig0025"></elsevierMultimedia><p id="par0055" class="elsevierStylePara elsevierViewall">Currently, laboratory techniques such as polymerase chain reaction (PCR), immunodiffusion, and complement fixation can be used to identify reactive antibodies. These tests are positive in 90% of the patients with acute pulmonary histoplasmosis without immunosuppression, although they are often negative in patients with AIDS.<a class="elsevierStyleCrossRef" href="#bib0075"><span class="elsevierStyleSup">15</span></a></p><p id="par0060" class="elsevierStylePara elsevierViewall">Finally, we should remember that measurement of a polysaccharide antigen in serum and urine is the most sensitive and rapid test, although it may yield false positives in patients with other mycotic diseases, particularly blastomycosis.<a class="elsevierStyleCrossRefs" href="#bib0075"><span class="elsevierStyleSup">15,16</span></a></p><p id="par0065" class="elsevierStylePara elsevierViewall">Imaging tests may not be positive in patients with disseminated histoplasmosis. Thus, <span class="elsevierStyleItalic">H capsulatum</span> has been isolated from the lungs of patients with AIDS, and so a negative result does not rule out the disease. Imaging is used essentially to determine the extent of disease (<a class="elsevierStyleCrossRef" href="#fig0030">Fig. 6</a>).</p><elsevierMultimedia ident="fig0030"></elsevierMultimedia></span><span id="sec0045" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0065">Differential Diagnosis</span><p id="par0070" class="elsevierStylePara elsevierViewall">Differential diagnosis includes conditions such as secondary syphilis and molluscum contagiosum (<a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>).<a class="elsevierStyleCrossRefs" href="#bib0080"><span class="elsevierStyleSup">16,17</span></a></p><elsevierMultimedia ident="tbl0005"></elsevierMultimedia></span><span id="sec0050" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0070">Treatment and Outcome</span><p id="par0075" class="elsevierStylePara elsevierViewall">The international guidelines for treatment of histoplasmosis in patients with AIDS have changed since the introduction of ART. In fact, such therapy is considered fundamental for the prevention and control of opportunistic mycoses in these patients (<a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>).<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">9</span></a></p></span></span><span id="sec0055" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0075">Coccidioidomycosis</span><span id="sec0060" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0080">Etiology</span><p id="par0080" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">Coccidioides</span> species are an imperfect dimorphic fungus. As a parasite, this organism takes the form of a spherule with endospores, whereas the saprophytic form is a mold with a septate mycelium that produces thallic conidia. The mycelium alternates between disjunctor, degenerate, and empty cells. Coccidioidomycosis is a systemic mycosis caused by microorganisms of the <span class="elsevierStyleItalic">Coccidioides</span> genus, which includes 2 species, <span class="elsevierStyleItalic">C immitis</span> and <span class="elsevierStyleItalic">Coccidioides posadasii.</span><a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a></p></span><span id="sec0065" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0085">Transmission Mechanism</span><p id="par0085" class="elsevierStylePara elsevierViewall">Infection is acquired through inhalation of arthrospores from soil or laboratory cultures. Once inhaled, the spores become lodged in the pulmonary alveoli and activate the host's first line of defense, comprising polymorphonuclear cells and macrophages. The complement system is also activated. The macrophages engulf the conidia but lysis does not occur until activation by type 1 T helper cells. Eosinophils and mastocytes are also activated, releasing large amounts of immunoglobulin E. The fungus, in addition to having a high biotic potential (each spherule can produce up to 800 endospores), has defense mechanisms to protect it from the host’ immune response. These defense mechanisms include production of metalloproteinase 1, which degrades a protein on the surface of the endospores (spherule outer wall glycoprotein). As this glycoprotein interacts with the antibodies to trigger opsonization of the parasite, its production enables the pathogen to elude recognition by the immune system and persist in the host. <span class="elsevierStyleItalic">C posadasii</span> produces ammonia, which favors infection by increasing the pH in infected tissues. In vivo experiments have shown that the microorganism can synthesize melanin.<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a></p><p id="par0090" class="elsevierStylePara elsevierViewall">Infection is not transmitted from one person to another because it cannot be acquired from spores present in expectoration or exudate although perinatal transmission is possible. Infection of the genitourinary tract of the mother can cause infection of the placenta and coccidioidal endometriosis with aspiration of infected amniotic liquid and consequent intrauterine or perinatal transmission.<a class="elsevierStyleCrossRefs" href="#bib0090"><span class="elsevierStyleSup">18–22</span></a></p></span><span id="sec0070" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0090">Epidemiology</span><p id="par0095" class="elsevierStylePara elsevierViewall">Coccidioidomycosis is the most common and most serious respiratory mycosis. Per year, there are thought to be between 45 000 and 100 000 cases, 50% of which originate in the south of the United States.<a class="elsevierStyleCrossRefs" href="#bib0025"><span class="elsevierStyleSup">5,23</span></a> In the last 2 decades, several endemic areas have been identified: northwest Brazil, Mexico, Guatemala, Honduras, Venezuela, and Argentina.<a class="elsevierStyleCrossRef" href="#bib0120"><span class="elsevierStyleSup">24</span></a></p></span><span id="sec0075" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0095">Overview of Symptoms</span><p id="par0100" class="elsevierStylePara elsevierViewall">The first reports of AIDS-related coccidioidomycosis appeared a few years after the first reports of the syndrome itself. The course is progressive and can lead to severe respiratory failure.<a class="elsevierStyleCrossRefs" href="#bib0125"><span class="elsevierStyleSup">25–27</span></a></p><p id="par0105" class="elsevierStylePara elsevierViewall">Coccidioidomycosis has been detected in almost all organs: the eyes, larynx, thyroid glands, peritoneum, prostate, kidneys, and uterus, as well as in prostheses and peritoneal shunts. Bone involvement is uncommon. Vertebral discs are rarely affected, but paraspinal masses with fistulas are common. Other bones that may be affected include the cranium, ribs, tibia, femur, metacarpals, and metatarsals.</p><p id="par0110" class="elsevierStylePara elsevierViewall">Dissemination to the CNS is the most serious form of infection. Such spread usually manifests as chronic granulomatous meningitis, with involvement of the basilar meninges; hydrocephaly may be present.<a class="elsevierStyleCrossRefs" href="#bib0140"><span class="elsevierStyleSup">28,29</span></a></p></span><span id="sec0080" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0100">Skin Manifestations</span><p id="par0115" class="elsevierStylePara elsevierViewall">The skin is the structure most commonly involved when disease is disseminated. Manifestations are varied and lesions may coalesce to form plaques (<a class="elsevierStyleCrossRefs" href="#fig0035">Figs. 7 and 8</a>). The granulomatous lesions show minimal inflammation. With ulcerated lesions, the possibility of a fistula should be considered.<a class="elsevierStyleCrossRef" href="#bib0150"><span class="elsevierStyleSup">30</span></a></p><elsevierMultimedia ident="fig0035"></elsevierMultimedia><elsevierMultimedia ident="fig0040"></elsevierMultimedia></span><span id="sec0085" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0105">Laboratory Tests and Imaging</span><p id="par0120" class="elsevierStylePara elsevierViewall">Diagnosis is based on intradermal reactions to coccidioidin or spherulin, which is the most sensitive agent. The test is positive from between 2 days to 3 weeks after infection and remains positive for several years.<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a> Imaging is negative in up to 98% of patients with AIDS in the first 48 to 72<span class="elsevierStyleHsp" style=""></span>hours.<a class="elsevierStyleCrossRef" href="#bib0130"><span class="elsevierStyleSup">26</span></a></p><p id="par0125" class="elsevierStylePara elsevierViewall">Serology tests are less reliable in HIV-infected patients, although they are positive in 68% to 74% of cases. However, enzyme-linked immunosorbent assay and complement fixing show high sensitivity. Tube precipitation tests are very specific. Binding of particles to latex is positive in 70% of cases.</p><p id="par0130" class="elsevierStylePara elsevierViewall">Techniques such as fluorescent antibodies, monoclonal antibodies, PCR, and in situ hybridization can also be used for detection.</p><p id="par0135" class="elsevierStylePara elsevierViewall">Cultures can be obtained in secure laboratories equipped to handle hazardous materials. Microscopic analysis reveals slender, septate hyphae with rectangular arthrospores.<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a></p><p id="par0140" class="elsevierStylePara elsevierViewall">Hematoxylin and eosin staining of biopsy samples from skin lesions and lesions in other tissues (<a class="elsevierStyleCrossRef" href="#fig0045">Fig. 9</a>) often reveals spherules measuring 10 to 80<span class="elsevierStyleHsp" style=""></span>μm, with a doubly refractile wall and endospores measuring 2 to 5<span class="elsevierStyleHsp" style=""></span>μm. However, these structures can be visualized better with PAS and Gomori-Grocott stains (<a class="elsevierStyleCrossRef" href="#fig0050">Fig. 10</a>). Histopathology also reveals a granulomatous reaction around the spherules.<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a></p><elsevierMultimedia ident="fig0045"></elsevierMultimedia><elsevierMultimedia ident="fig0050"></elsevierMultimedia><p id="par0145" class="elsevierStylePara elsevierViewall">The fungus can be isolated in cerebrospinal fluid (CSF) in only half the cases: diagnosis is confirmed with a positive finding for immunoglobulin G antibodies.<a class="elsevierStyleCrossRef" href="#bib0130"><span class="elsevierStyleSup">26</span></a> Radiographic studies are not specific for coccidioidomycosis.<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a></p></span><span id="sec0090" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0110">Differential Diagnosis</span><p id="par0150" class="elsevierStylePara elsevierViewall">The differential diagnosis should initially include tuberculosis in its different clinical manifestations and then consider sporotrichosis, among other conditions (<a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>).<a class="elsevierStyleCrossRef" href="#bib0155"><span class="elsevierStyleSup">31</span></a></p></span><span id="sec0095" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0115">Treatment</span><p id="par0155" class="elsevierStylePara elsevierViewall">Treatment for the different forms of coccidioidomycosis is subject to debate. Given the widely variable results and limited number of controlled studies, it is hard to propose universal recommendations for the treatment of each clinical manifestation in HIV-infected patients, particularly regarding the duration of therapy (<a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>). In a patient with disseminated coccidioidomycosis, successful use of interferon gamma at a dose of 50<span class="elsevierStyleHsp" style=""></span>μg/m<span class="elsevierStyleSup">2</span>, 3 times a week, has been reported.<a class="elsevierStyleCrossRef" href="#bib0145"><span class="elsevierStyleSup">29</span></a> Patients with initially negative serology may experience a delay in improvement and the findings do not necessarily correlate with disease course. The duration of therapy has not been defined, although treatment for at least 1 year is recommended.<a class="elsevierStyleCrossRefs" href="#bib0160"><span class="elsevierStyleSup">32,33</span></a></p></span></span><span id="sec0100" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0120">Cryptococcosis</span><span id="sec0105" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0125">Etiology</span><p id="par0160" class="elsevierStylePara elsevierViewall">The <span class="elsevierStyleItalic">Cryptococcus</span> genus includes many species. Of these, human infection only occurs with <span class="elsevierStyleItalic">Cryptococcus neoformans</span> (variant <span class="elsevierStyleItalic">neoformans</span> and variant <span class="elsevierStyleItalic">grubii</span>) and <span class="elsevierStyleItalic">Cryptococcus gattii</span>, of which 5 serotypes—A, B, C, D, and AD—have been identified.<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> These microorganisms have a firm wall and a spherical or elliptical shape. Characteristically, they have a thick capsule that can be stained with freshly prepared India ink. The capsule is composed of polysaccharides, mainly glucuronoxylomannan (90%–95%), galactoxylomannan (5%–8%), and mannoproteins (<<span class="elsevierStyleHsp" style=""></span>1%).<a class="elsevierStyleCrossRef" href="#bib0170"><span class="elsevierStyleSup">34</span></a></p></span><span id="sec0110" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0130">Transmission Mechanism</span><p id="par0165" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">C neoformans</span> is ubiquitous in the urban environment and is found in pigeon excrement and, to a lesser extent, bat excrement, whereas <span class="elsevierStyleItalic">C gattii</span> has been associated with certain trees and is limited to tropical and subtropical regions.<a class="elsevierStyleCrossRefs" href="#bib0170"><span class="elsevierStyleSup">34–38</span></a> Penetration occurs mainly via the respiratory tract and, more rarely, via the gastrointestinal tract and the skin.<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a> Once inside the host, the yeast can change the composition and size of the capsule to increase its chances of resisting or eluding the host's defense mechanisms. These changes determine the principal virulence factor of the microorganism, which confers an ability to avoid phagocytosis, change its phenotype, and, in some cases, produce melanin.<a class="elsevierStyleCrossRef" href="#bib0195"><span class="elsevierStyleSup">39</span></a></p></span><span id="sec0115" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0135">Epidemiology</span><p id="par0170" class="elsevierStylePara elsevierViewall">Cryptococcosis is a common opportunistic infection in patients with HIV infection/AIDS; in fact, it is the most frequent disseminated fungal infection in these cases. Immune cell dysfunction is considered the main risk factor so patients with HIV infection/AIDS are highly susceptible despite treatment with ART.<a class="elsevierStyleCrossRef" href="#bib0200"><span class="elsevierStyleSup">40</span></a></p><p id="par0175" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">C neoformans</span> variant <span class="elsevierStyleItalic">neoformans</span> (serotype D) and especially the variant <span class="elsevierStyleItalic">grubii</span> (serotype A) is the species implicated in the infection of immunocompromised patients, including those with HIV infection or cancer and solid-organ transplant recipients.<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a><span class="elsevierStyleItalic">C</span> <span class="elsevierStyleItalic">gattii</span> has recently been described as an emerging species in the northwest region of North America, although mainly immunocompetent patients are infected.</p><p id="par0180" class="elsevierStylePara elsevierViewall">In Europe, <span class="elsevierStyleItalic">C neoformans</span> is the cause of 20% of infections in patients with HIV infection/AIDS. In Africa, it is the initial infection in 20% to 30% of patients and responsible for 20% to 40% of deaths attributable to AIDS. Extrapulmonary cryptococcosis is even considered a defining infection of AIDS; this form is detected in 4.3% of cases and presents more frequently in the skin, prostate, and eyes. Cryptococcal meningitis is more common in patients with CD4<span class="elsevierStyleSup">+</span><span class="elsevierStyleHsp" style=""></span>cell counts below<span class="elsevierStyleHsp" style=""></span>100 cells/μL.<a class="elsevierStyleCrossRef" href="#bib0205"><span class="elsevierStyleSup">41</span></a></p></span><span id="sec0120" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0140">Overview of Symptoms</span><p id="par0185" class="elsevierStylePara elsevierViewall">Cryptococcosis causes pneumonia in most cases, but pulmonary cryptococcomas have also been reported and, in 10% of patients, hematogenous spread may occur to other organs, mainly the CNS. Often, on diagnosis, infection is disseminated and meningitis is present in up to 60% to 70% of patients. The onset of meningitis is insidious, with impaired hearing and higher-level mental processes, headache, fatigue, dizziness, irritability, and/or impaired coordination. Other organs that may be infected include the kidney, liver, and genitourinary tract. The skeletal system may also become involved.<a class="elsevierStyleCrossRef" href="#bib0210"><span class="elsevierStyleSup">42</span></a></p></span><span id="sec0125" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0145">Skin Manifestations</span><p id="par0190" class="elsevierStylePara elsevierViewall">Skin lesions, which are present in 10% to 15% of patients, may be single or multiple and appear predominantly on the trunk and face (<a class="elsevierStyleCrossRefs" href="#fig0055">Figs. 11 and 12</a>). The clinical presentation is extremely varied. Skin lesions may arise from disseminated <span class="elsevierStyleItalic">C immitis</span> infection, from old quiescent pulmonary lesions that are reactivated when the effectiveness of specific immune mechanisms are undermined, or from propagation of the pathogen from underlying lymph node, skeletal, or articular lesions. Usually, multiple lesions develop, with the first ones appearing on the head and neck (near natural orifices). Subsequently, they coalesce to form plaques and become verrucous. Cutaneous granulomas appear in the vicinity of fistulous tracts, which tend to heal while the lesion progresses at the borders. In other cases, chronic bone lesions induce secondary involvement of soft tissue. The most characteristic lesions are described in <a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>.<a class="elsevierStyleCrossRefs" href="#bib0215"><span class="elsevierStyleSup">43,44</span></a></p><elsevierMultimedia ident="fig0055"></elsevierMultimedia><elsevierMultimedia ident="fig0060"></elsevierMultimedia></span></span><span id="sec0130" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0150">Laboratory Tests and Imaging</span><p id="par0195" class="elsevierStylePara elsevierViewall">The cryptococcus can usually be identified by laboratory analysis of blood, bone marrow, CSF, and samples from the eye, respiratory tract, skin and mucosae, urine, and other tissues. From any patient who is positive for the cryptococcal antigen, in whom encapsulated yeasts are detected in direct examination or histology, or in whom <span class="elsevierStyleItalic">C neoformans</span> is isolated from any other body site, it is recommended to obtain, immediately inspect, and culture samples from the CSF, blood, urine, and serum. This process will enable the assessment of the severity of infection and the optimal induction of treatment.<a class="elsevierStyleCrossRefs" href="#bib0025"><span class="elsevierStyleSup">5,45</span></a></p><p id="par0200" class="elsevierStylePara elsevierViewall">The India ink test can be performed with any body fluid. Yeasts measuring 2 to 5<span class="elsevierStyleHsp" style=""></span>μm are observed to be surrounded by a mucoid capsule that remains unstained (<a class="elsevierStyleCrossRef" href="#fig0065">Fig. 13</a>). This test is quick (taking less than a minute) and very specific though sensitivity is low as only 50% of cases are positive.<a class="elsevierStyleCrossRef" href="#bib0230"><span class="elsevierStyleSup">46</span></a></p><elsevierMultimedia ident="fig0065"></elsevierMultimedia><p id="par0205" class="elsevierStylePara elsevierViewall">Tissue sections can be stained to facilitate visualization of the fungus. The most useful stains are PAS, Grocott, Papanicolaou, and Gram. For diagnosis of clinical samples, the fungus can be also be inspected by fluorescence microscopy with calcofluor-white staining or phase contrast microscopy.<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a></p><p id="par0210" class="elsevierStylePara elsevierViewall">Any tissue or body fluid can be cultured. The fungi grow in temperatures ranging from 25<span class="elsevierStyleHsp" style=""></span>°C to 37<span class="elsevierStyleHsp" style=""></span>°C and the yeast colonies can be white, yellow, or light-coffee colored. A cryptococcal species is definitively identified be means of the carbohydrate utilization test and production of pigment on Niger agar (<span class="elsevierStyleItalic">Gyzotia abissinica</span>).<a class="elsevierStyleCrossRef" href="#bib0235"><span class="elsevierStyleSup">47</span></a></p><span id="sec0135" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0155">Differential Diagnosis</span><p id="par0215" class="elsevierStylePara elsevierViewall">Differential diagnosis should include molluscum contagiosum, herpes simplex virus, rhinophyma, Kaposi sarcoma, and bacterial cellulitis (<a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>).<a class="elsevierStyleCrossRefs" href="#bib0200"><span class="elsevierStyleSup">40–42</span></a></p></span><span id="sec0140" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0160">Treatment and Follow-up</span><p id="par0220" class="elsevierStylePara elsevierViewall">The treatment of choice for disseminated infection is a combination of intravenous amphotericin B and flucytosine. This combination allows the dose of both drugs to be reduced, thereby lowering toxicity and side effects. It is important to remember that flucytosine increases hematologic toxicity in patients receiving treatment with zidovudine, so renal function and flucytosine levels should be closely monitored (<a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>). Two predictive factors for mortality have been proposed: a CD4<span class="elsevierStyleSup">+</span> count less than 50 cells/μL and a history of oral candidiasis prior to starting ART.<a class="elsevierStyleCrossRefs" href="#bib0210"><span class="elsevierStyleSup">42,43</span></a></p></span></span><span id="sec0145" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0165">Skin Manifestations and Immune Reconstitution Inflammatory Syndrome</span><p id="par0225" class="elsevierStylePara elsevierViewall">With the introduction of highly active antiretroviral therapy (HAART), the incidence of many opportunistic infections has decreased in HIV-infected patients. At the same time though, these agents have brought new problems, such as immune reconstitution inflammatory syndrome (IRIS), an adverse effect of HAART-induced reconstitution of the antigen-specific immune response that is manifest as the clinical onset of preexisting subclinical infections or the vigorous onset of autoimmune and neoplastic diseases.<a class="elsevierStyleCrossRefs" href="#bib0240"><span class="elsevierStyleSup">48–50</span></a></p><p id="par0230" class="elsevierStylePara elsevierViewall">Cases of skin manifestations of histoplasmosis have been reported. In most cases, the patients presented with generalized papular or crusty lesions (<a class="elsevierStyleCrossRef" href="#fig0070">Fig. 14</a>) and, in 1 case in particular the patient had a nodular lesion on the face, with accompanying fever and lymphadenitis. Histology of samples from skin and lymph nodes showed giant cell granulomas with necrosis and yeast cells. <span class="elsevierStyleItalic">H capsulatum</span> was cultured from blood samples and this microorganism was also isolated from skin and the lungs. The treatment is the same antifungal therapy as described above.<a class="elsevierStyleCrossRef" href="#bib0255"><span class="elsevierStyleSup">51</span></a></p><elsevierMultimedia ident="fig0070"></elsevierMultimedia><p id="par0235" class="elsevierStylePara elsevierViewall">The exact incidence of <span class="elsevierStyleItalic">C neoformans</span>-related IRIS is not known even though this microorganism is always detected in series and case reports of patients with IRIS. In most cases, the cause is reactivation of previously treated infections, suggesting that the condition is an immune response to inadequately treated disease or an inflammatory reaction to certain residual antigens. IRIS presents mostly in the form of meningitis, although cases presenting as lymphadenitis and mediastinitis have also been reported.</p><p id="par0240" class="elsevierStylePara elsevierViewall">Skin manifestations are uncommon, but when present they appear as large single or multiple masses or large ulcers. In some cases, surgery is required to excise the nodular lesions while HAART continues.<a class="elsevierStyleCrossRef" href="#bib0260"><span class="elsevierStyleSup">52</span></a></p><p id="par0245" class="elsevierStylePara elsevierViewall">There have been no reports of IRIS in patients with HIV/AIDS and coccidioidomycosis.</p></span><span id="sec0150" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0170">Practical Consequences in Spain</span><p id="par0250" class="elsevierStylePara elsevierViewall">Dermatologists should be prepared to detect rare diseases and atypical presentations of the most common infections—skin infections in particular—in patients with a compromised immune system, including those with HIV infection/AIDS. The impairment and dysregulation of immunity caused by HIV makes patients are susceptible to a wide range of skin infections. Lesions may show less inflammation than is usual or be more generalized, disfiguring, and destructive. Lesions can also be atypical when HIV-infected patients develop lesions caused by simultaneous infection of more than a single pathogen.<a class="elsevierStyleCrossRef" href="#bib0265"><span class="elsevierStyleSup">53</span></a></p><p id="par0255" class="elsevierStylePara elsevierViewall">Histoplasmosis is a common opportunistic infection in HIV-infected patients who live in endemic areas. Mortality can be as high as 80% according to some reports. Although uncommon in Europe, and particularly in Spain, some cases are still seen mainly because of the increasing number of immigrants and visitors from endemic countries such as eastern United States of America, Latin America, sub-Saharan Africa, east Asia, and Oceania.<a class="elsevierStyleCrossRef" href="#bib0265"><span class="elsevierStyleSup">53</span></a> When HIV-infected individuals seek our care, histoplasmosis is present in disseminated form in 95%.<a class="elsevierStyleCrossRef" href="#bib0270"><span class="elsevierStyleSup">54</span></a> The skin lesions arise as a result of hematogenous spread and onset generally occurs after the CD4<span class="elsevierStyleSup">+</span> cell count has fallen below 150 cells/μL.</p><p id="par0260" class="elsevierStylePara elsevierViewall">Different strains of <span class="elsevierStyleItalic">H capsulatum</span> have been identified, in relation to whether the patient has AIDS or not. Reyes-Montes et al.<a class="elsevierStyleCrossRef" href="#bib0275"><span class="elsevierStyleSup">55</span></a> isolated the following chain types from <span class="elsevierStyleItalic">H capsulatum</span> in Mexican patients with AIDS: EH-316, EH-317, EH-318, EH-319, EH-323, and EH-325. In contrast, EH-46 and EH-53 were isolated from patients without AIDS.</p><p id="par0265" class="elsevierStylePara elsevierViewall">Whether or not sex is a risk factor for disease is still under debate. Some authors report that histoplasmosis affects men and women in equal measure whereas others have found predominance among men. There is little information about the incidence of histoplasmosis between different ethnic groups or races. However, many authors seem to agree that the features of the skin lesions may differ with race and endemic status of the region.</p><p id="par0270" class="elsevierStylePara elsevierViewall">The first cases of disseminated histoplasmosis with skin involvement were reported by Bayes et al.<a class="elsevierStyleCrossRefs" href="#bib0280"><span class="elsevierStyleSup">56–59</span></a> Subsequently, other investigators reported further cases.<a class="elsevierStyleCrossRefs" href="#bib0300"><span class="elsevierStyleSup">60,61</span></a> After reviewing the literature, we found that the most common sites for lesions, in decreasing order, were the face and scalp, legs, shoulders and back, trunk, neck, and abdomen<a class="elsevierStyleCrossRefs" href="#bib0045"><span class="elsevierStyleSup">9,16,17,57–62</span></a> (<a class="elsevierStyleCrossRef" href="#fig0075">Fig. 15</a>). However, Bonifaz and Chang<a class="elsevierStyleCrossRef" href="#bib0315"><span class="elsevierStyleSup">63</span></a> found that lesions occur mainly on the face and trunk. Cutaneous lesions are present in 38% to 85% of cases, according to whether patients are originally from South America or Africa, suggesting that genetic differences are present in these 2 variants. It has been suggested that dermotropic strains of <span class="elsevierStyleItalic">H capsulatum</span> may be responsible for the higher frequency of skin lesions in patients with AIDS. <span class="elsevierStyleItalic">H capsulatum</span> has been found in endoneural macrophages and in Schwann cells in cutaneous nerves. It is thought that a large number of these microorganisms invade the dermis, with secondary nerve infection then occurring although affected nerves do not show necrosis or cell proliferation. The presence of fungal elements in cutaneous nerves could be the main indicator of recurrent disease or dissemination. Mucosal lesions such as papules, nodules, and ulcers may occur in the gastrointestinal tract.</p><elsevierMultimedia ident="fig0075"></elsevierMultimedia><p id="par0275" class="elsevierStylePara elsevierViewall">Bonifaz and Chang<a class="elsevierStyleCrossRef" href="#bib0315"><span class="elsevierStyleSup">63</span></a> found papules, nodules and hyperkeratotic plaques, some ulcers, and purpuric lesions in all their patients. This clinical presentation occurs frequently and had been reported previously in populations in Latin America.<a class="elsevierStyleCrossRefs" href="#bib0060"><span class="elsevierStyleSup">12,64</span></a> Samples taken by curettage of these lesions lead to confirmation of the diagnosis of mycosis in almost all cases.<a class="elsevierStyleCrossRef" href="#bib0320"><span class="elsevierStyleSup">64</span></a></p><p id="par0280" class="elsevierStylePara elsevierViewall">Of note is that primary prophylaxis (itraconazole, 200<span class="elsevierStyleHsp" style=""></span>mg/d) is administered to HIV-positive patients with a CD4<span class="elsevierStyleSup">+</span> count less than 150 cells/μL. A mortality rate of 43.5% has been reported in patients with disease that has become disseminated despite treatment,<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">8</span></a> whereas in a recent European review this figure was 15% in the initial phases of treatment and 57% during follow-up.<a class="elsevierStyleCrossRef" href="#bib0325"><span class="elsevierStyleSup">65</span></a></p><p id="par0285" class="elsevierStylePara elsevierViewall">Coccidioidomycosis is a systemic mycosis found in America. The disseminated form is most common in men and in patients with AIDS and with dark skin. The course of infection may be acute, subacute, or chronic. In the subacute and chronic forms, most symptoms are localized to the skin, subcutaneous tissue, osteoarticular system, lymph nodes, and the CNS.</p><p id="par0290" class="elsevierStylePara elsevierViewall">The primary pulmonary form manifests as pneumonia (in 44%) and miliary involvement may be present (in 19%). Cavitation or coccidioidomas may also be present (in 19%).<a class="elsevierStyleCrossRefs" href="#bib0105"><span class="elsevierStyleSup">21,22,66</span></a> In approximately 0.2% of patients with primary pulmonary coccidioidomycosis, the lesions spread predominantly to the skin, CNS, and osteoarticular system. The disseminated form generally follows an acute course, reaching various organs and systems and rapidly leading to death if diagnosis and treatment are delayed. The first report of HIV-associated coccidioidomycosis in Spain appeared in 1997.<a class="elsevierStyleCrossRef" href="#bib0335"><span class="elsevierStyleSup">67</span></a> Approximately 10% to 20% of HIV-positive patients with systemic infection have cutaneous lesions, which provide a defining characteristic of AIDS and are a sign of poor prognosis. Early detection of these lesions can lead to early start of ART and so improve the prognosis.<a class="elsevierStyleCrossRef" href="#bib0330"><span class="elsevierStyleSup">66</span></a></p><p id="par0295" class="elsevierStylePara elsevierViewall">The large number of clinical forms and possible complications make it difficult to indicate specific treatment regimens for every situation. Recently, in cases refractory to treatment, voriconazole and posaconazole have been suggested for their broad spectrum of action, but outcomes have not been very satisfactory.<a class="elsevierStyleCrossRef" href="#bib0340"><span class="elsevierStyleSup">68</span></a></p><p id="par0300" class="elsevierStylePara elsevierViewall">Although vaccines against coccidioidomycoses have been under investigation for years, none as yet has proven effective. Vaccines based on total RNA extracted from spherules have been shown to be ineffective. However, in recent studies, recombinant antigens have shown promising results in animal models.<a class="elsevierStyleCrossRefs" href="#bib0090"><span class="elsevierStyleSup">18,42</span></a></p><p id="par0305" class="elsevierStylePara elsevierViewall">Surgical resection of the lesion is indicated in cases of nodules in the lungs and at other sites when patients do not respond to antifungal therapy. Detection of a mass or abscess in the brain requires drainage or surgical resection. Debridement of cutaneous lesions to eliminate necrotic material is an important auxiliary measure. Patients should be treated in an outpatient setting, with follow-up at 3 and 6 months, then annually for a further 12 years.<a class="elsevierStyleCrossRef" href="#bib0160"><span class="elsevierStyleSup">32</span></a></p><p id="par0310" class="elsevierStylePara elsevierViewall">The virulence of the <span class="elsevierStyleItalic">Cryptococcus</span> genus is related to protease and oxidase production as well as the antiphagocytic properties of the capsular polysaccharide. The most plausible explanation for infection is the small diameter of the basidiospores (1.2–1.8<span class="elsevierStyleHsp" style=""></span>μm), which allows them to accumulate in the alveoli, where the encapsulated yeasts are transformed at a temperature of 37<span class="elsevierStyleHsp" style=""></span>°C. In most cases, inhalation of <span class="elsevierStyleItalic">Cryptococcus</span> species causes asymptomatic and self-limiting pulmonary infection, and yeasts can remain latent in the pulmonary environment or die. If an immunocompromised state develops subsequently, they may become reactivated and cause disease.<a class="elsevierStyleCrossRef" href="#bib0345"><span class="elsevierStyleSup">69</span></a> Several studies have shown that <span class="elsevierStyleItalic">C neoformans</span> molecular type VNI is predominant in HIV-positive patients whereas <span class="elsevierStyleItalic">C gattii</span> molecular type VGII is predominant in HIV-negative ones (<span class="elsevierStyleItalic">P</span><span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>.001). Only 3 out of 37 cases in HIV-positive patients (8.1%) were caused by <span class="elsevierStyleItalic">C gattii</span> molecular type VGII, whereas 5 of 21 cases in HIV-negative patients (23.8%) were caused by <span class="elsevierStyleItalic">C neoformans</span> molecular type VNI.<a class="elsevierStyleCrossRefs" href="#bib0350"><span class="elsevierStyleSup">70–72</span></a></p><p id="par0315" class="elsevierStylePara elsevierViewall">Before ART became available, cryptococcosis had become a major opportunistic infection and the leading cause of death in HIV-infected patients with CD4<span class="elsevierStyleSup">+</span> counts below 100<span class="elsevierStyleHsp" style=""></span>cells/μL.<a class="elsevierStyleCrossRefs" href="#bib0025"><span class="elsevierStyleSup">5,43</span></a> In Spain, cryptococcosis was the most common fungal infection in these patients as of 2006.<a class="elsevierStyleCrossRef" href="#bib0365"><span class="elsevierStyleSup">73</span></a></p><p id="par0320" class="elsevierStylePara elsevierViewall">Skin infection in cryptococcosis occurs in 10% to 20% of cases, almost always secondary to systemic infection and so is considered a “sentinel sign” of disseminated disease. Necrotizing infections in soft tissues (cellulitis and necrotizing fascitis) and lesions that resemble pyoderma gangrenosum and keloid scars have occasionally been reported. Mortality is high (80%).<a class="elsevierStyleCrossRefs" href="#bib0370"><span class="elsevierStyleSup">74,75</span></a></p><p id="par0325" class="elsevierStylePara elsevierViewall">Primary cutaneous cryptococcosis is a very rare condition, defined in the literature by the identification of <span class="elsevierStyleItalic">C neoformans</span> in a skin biopsy or culture in absence of disseminated disease. The sporotrichotic pattern is an extremely uncommon presentation. The patients in the cases we reviewed were immunocompromised but were not infected with HIV.<a class="elsevierStyleCrossRef" href="#bib0380"><span class="elsevierStyleSup">76</span></a></p><p id="par0330" class="elsevierStylePara elsevierViewall">The use of primary prophylaxis is still under discussion. In a metaanalysis of primary prophylaxis with fluconazole or itraconazole in HIV-infected patients with CD4<span class="elsevierStyleSup">+</span> counts below 300 cells/μL, the incidence of cryptococcosis decreased but mortality was unaffected. In patients with HAART-induced immune reconstitution, fluconazole or itraconazole can be interrupted provided the CD4<span class="elsevierStyleSup">+</span> count has remained stable above 100 cells/μL over the last 12 months.<a class="elsevierStyleCrossRefs" href="#bib0385"><span class="elsevierStyleSup">77,78</span></a></p></span><span id="sec0155" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0175">Conclusions</span><p id="par0335" class="elsevierStylePara elsevierViewall">Systemic mycoses are mainly pulmonary diseases caused by dimorphic pathogenic fungi. If the inoculum is large or the individual's immune system is compromised, primary infection is possible and may be acute, self-limiting, or subclinical. Most skin manifestations correspond to disseminated disease, and so systemic treatment is required. Given that other skin lesions may also develop in the course of these diseases, it is recommended to take an extensive medical history and perform additional imaging tests, accompanied by histopathologic study and culture.</p></span><span id="sec0160" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0180">Conflicts of Interest</span><p id="par0340" class="elsevierStylePara elsevierViewall">The authors declare that they have no conflicts of interest.</p></span></span>" "textoCompletoSecciones" => array:1 [ "secciones" => array:14 [ 0 => array:2 [ "identificador" => "xres304923" "titulo" => "Abstract" ] 1 => array:2 [ "identificador" => "xpalclavsec288080" "titulo" => "Keywords" ] 2 => array:2 [ "identificador" => "xres304924" "titulo" => "Resumen" ] 3 => array:2 [ "identificador" => "xpalclavsec288079" "titulo" => "Palabras clave" ] 4 => array:2 [ "identificador" => "sec0005" "titulo" => "Introduction" ] 5 => array:3 [ "identificador" => "sec0010" "titulo" => "Histoplasmosis" "secciones" => array:8 [ 0 => array:2 [ "identificador" => "sec0015" "titulo" => "Etiology" ] 1 => array:2 [ "identificador" => "sec0020" "titulo" => "Transmission Mechanism" ] 2 => array:2 [ "identificador" => "sec0025" "titulo" => "Epidemiology" ] 3 => array:2 [ "identificador" => "sec0030" "titulo" => "Overview of Symptoms" ] 4 => array:2 [ "identificador" => "sec0035" "titulo" => "Skin Manifestations" ] 5 => array:2 [ "identificador" => "sec0040" "titulo" => "Laboratory Tests and Imaging" ] 6 => array:2 [ "identificador" => "sec0045" "titulo" => "Differential Diagnosis" ] 7 => array:2 [ "identificador" => "sec0050" "titulo" => "Treatment and Outcome" ] ] ] 6 => array:3 [ "identificador" => "sec0055" "titulo" => "Coccidioidomycosis" "secciones" => array:8 [ 0 => array:2 [ "identificador" => "sec0060" "titulo" => "Etiology" ] 1 => array:2 [ "identificador" => "sec0065" "titulo" => "Transmission Mechanism" ] 2 => array:2 [ "identificador" => "sec0070" "titulo" => "Epidemiology" ] 3 => array:2 [ "identificador" => "sec0075" "titulo" => "Overview of Symptoms" ] 4 => array:2 [ "identificador" => "sec0080" "titulo" => "Skin Manifestations" ] 5 => array:2 [ "identificador" => "sec0085" "titulo" => "Laboratory Tests and Imaging" ] 6 => array:2 [ "identificador" => "sec0090" "titulo" => "Differential Diagnosis" ] 7 => array:2 [ "identificador" => "sec0095" "titulo" => "Treatment" ] ] ] 7 => array:3 [ "identificador" => "sec0100" "titulo" => "Cryptococcosis" "secciones" => array:5 [ 0 => array:2 [ "identificador" => "sec0105" "titulo" => "Etiology" ] 1 => array:2 [ "identificador" => "sec0110" "titulo" => "Transmission Mechanism" ] 2 => array:2 [ "identificador" => "sec0115" "titulo" => "Epidemiology" ] 3 => array:2 [ "identificador" => "sec0120" "titulo" => "Overview of Symptoms" ] 4 => array:2 [ "identificador" => "sec0125" "titulo" => "Skin Manifestations" ] ] ] 8 => array:3 [ "identificador" => "sec0130" "titulo" => "Laboratory Tests and Imaging" "secciones" => array:2 [ 0 => array:2 [ "identificador" => "sec0135" "titulo" => "Differential Diagnosis" ] 1 => array:2 [ "identificador" => "sec0140" "titulo" => "Treatment and Follow-up" ] ] ] 9 => array:2 [ "identificador" => "sec0145" "titulo" => "Skin Manifestations and Immune Reconstitution Inflammatory Syndrome" ] 10 => array:2 [ "identificador" => "sec0150" "titulo" => "Practical Consequences in Spain" ] 11 => array:2 [ "identificador" => "sec0155" "titulo" => "Conclusions" ] 12 => array:2 [ "identificador" => "sec0160" "titulo" => "Conflicts of Interest" ] 13 => array:1 [ "titulo" => "References" ] ] ] "pdfFichero" => "main.pdf" "tienePdf" => true "fechaRecibido" => "2011-07-29" "fechaAceptado" => "2012-06-24" "PalabrasClave" => array:2 [ "en" => array:1 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Keywords" "identificador" => "xpalclavsec288080" "palabras" => array:5 [ 0 => "Coccidioidomycosis" 1 => "Cryptococcosis" 2 => "Histoplasmosis" 3 => "Adquired inmunodeficiency syndrome" 4 => "Human immunodeficiency virus" ] ] ] "es" => array:1 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Palabras clave" "identificador" => "xpalclavsec288079" "palabras" => array:5 [ 0 => "Coccidioidomicosis" 1 => "Criptococosis" 2 => "Histoplasmosis" 3 => "Sida" 4 => "Virus de la inmunodeficiencia humana" ] ] ] ] "tieneResumen" => true "resumen" => array:2 [ "en" => array:2 [ "titulo" => "Abstract" "resumen" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Histoplasmosis is a systemic infection caused by the dimorphic fungus <span class="elsevierStyleItalic">Histoplasma capsulatum</span>. In immunocompromised patients, primary pulmonary infection can spread to the skin and meninges. Clinical manifestations appear in patients with a CD4<span class="elsevierStyleSup">+</span> lymphocyte count of less than 150 cells/μL.</p><p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">Coccidioidomycosis is a systemic mycosis caused by <span class="elsevierStyleItalic">Coccidioides immitis</span> and <span class="elsevierStyleItalic">Coccidioides posadasii</span>. It can present as diffuse pulmonary disease or as a disseminated form primarily affecting the central nervous system, the bones, and the skin.</p><p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">Cryptococcosis is caused by <span class="elsevierStyleItalic">Cryptococcus neoformans</span> (var. <span class="elsevierStyleItalic">neoformans</span> and var. <span class="elsevierStyleItalic">grubii</span>) and <span class="elsevierStyleItalic">Cryptococcus gattii</span>, which are members of the <span class="elsevierStyleItalic">Cryptococcus</span> species complex and have 5 serotypes: A, B, C, D, and AD. It is a common opportunistic infection in patients with human immunodeficiency virus (HIV)/AIDS, even those receiving antiretroviral therapy.</p><p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">Histopathologic examination and culture of samples from any suspicious lesions are essential for the correct diagnosis of systemic fungal infections in patients with HIV/AIDS.</p>" ] "es" => array:2 [ "titulo" => "Resumen" "resumen" => "<p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">La histoplasmosis es una micosis sistémica causada por el hongo dimorfo <span class="elsevierStyleItalic">Histoplasma capsulatum</span>. En pacientes inmunocomprometidos se produce una progresión de la enfermedad pulmonar y la diseminación en la piel y las meninges. Las manifestaciones clínicas aparecen cuando los niveles de linfocitos CD4 son menores a 150 células/μl.</p><p id="spar0030" class="elsevierStyleSimplePara elsevierViewall">La coccidioidomicosis es una micosis sistémica causada por <span class="elsevierStyleItalic">Coccidioides immitis</span> y <span class="elsevierStyleItalic">Coccidioides posadasii.</span> Se presenta como una forma pulmonar difusa o diseminada, con manifestaciones en el sistema nervioso central, los huesos y la piel, fundamentalmente.</p><p id="spar0035" class="elsevierStyleSimplePara elsevierViewall">La criptococosis está causada por diferentes especies de <span class="elsevierStyleItalic">Cryptococcus species complex</span>, <span class="elsevierStyleItalic">Cryptococcus neoformans</span> (var. <span class="elsevierStyleItalic">neoformans</span> y var. <span class="elsevierStyleItalic">grubii</span>) y <span class="elsevierStyleItalic">Cryptococcus gattii</span>, que conforman los 5 serotipos identificados: A, B, C, D y AD. Es una infección oportunista común en pacientes con VIH/sida, incluso si están en tratamiento con antirretrovirales.</p><p id="spar0040" class="elsevierStyleSimplePara elsevierViewall">El estudio histopatológico y el cultivo de cualquier lesión sospechosa son fundamentales para un correcto diagnóstico de estas micosis sistémicas en pacientes infectados por el VIH/sida.</p>" ] ] "NotaPie" => array:1 [ 0 => array:2 [ "etiqueta" => "☆" "nota" => "<p class="elsevierStyleNotepara" id="npar0005">Please cite this article as: Rodríguez-Cerdeira C, Arenas R, Moreno-Coutiño G, Vásquez E, Fernández R, Chang P. Micosis sistémicas en pacientes con virus de la inmunodeficiencia humana/sida. Actas Dermosifiliogr. 2014;105:5–17.</p>" ] ] "multimedia" => array:16 [ 0 => array:7 [ "identificador" => "fig0005" "etiqueta" => "Figure 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 668 "Ancho" => 900 "Tamanyo" => 67108 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0045" class="elsevierStyleSimplePara elsevierViewall">Papular erythematous-violaceous lesions on the leg of a patient with disseminated histoplasmosis and a CD4<span class="elsevierStyleSup">+</span> count <<span class="elsevierStyleHsp" style=""></span>150<span class="elsevierStyleHsp" style=""></span>cells/μL.</p>" ] ] 1 => array:7 [ "identificador" => "fig0010" "etiqueta" => "Figure 2" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr2.jpeg" "Alto" => 663 "Ancho" => 900 "Tamanyo" => 107560 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0050" class="elsevierStyleSimplePara elsevierViewall">Desquamative lesions, mainly on the face, with an ulcerated region in the philtrum, in a patient with disseminated histoplasmosis as the first manifestation of AIDS.</p>" ] ] 2 => array:7 [ "identificador" => "fig0015" "etiqueta" => "Figure 3" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr3.jpeg" "Alto" => 642 "Ancho" => 900 "Tamanyo" => 80996 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0055" class="elsevierStyleSimplePara elsevierViewall">Disseminated violaceous nonpruritic maculopapular lesions in a patient with disseminated histoplasmosis.</p>" ] ] 3 => array:7 [ "identificador" => "fig0020" "etiqueta" => "Figure 4" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr4.jpeg" "Alto" => 692 "Ancho" => 900 "Tamanyo" => 115152 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0060" class="elsevierStyleSimplePara elsevierViewall">Disseminated histoplasmosis with characteristic small ulcers on the palate.</p>" ] ] 4 => array:7 [ "identificador" => "fig0025" "etiqueta" => "Figure 5" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr5.jpeg" "Alto" => 548 "Ancho" => 900 "Tamanyo" => 114013 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0065" class="elsevierStyleSimplePara elsevierViewall">Numerous macrophages containing <span class="elsevierStyleItalic">Histoplasma capsulatum</span> yeasts in tissue from a patient with periodic acid-Schiff (PAS) positive histoplasmosis. PAS, original magnification<span class="elsevierStyleHsp" style=""></span>×100.</p>" ] ] 5 => array:7 [ "identificador" => "fig0030" "etiqueta" => "Figure 6" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr6.jpeg" "Alto" => 642 "Ancho" => 950 "Tamanyo" => 97674 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0070" class="elsevierStyleSimplePara elsevierViewall">Chest radiographs showing small interstitial nodules in both lungs in a patient positive for the human immunodeficiency virus with disseminated histoplasmosis.</p>" ] ] 6 => array:7 [ "identificador" => "fig0035" "etiqueta" => "Figure 7" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr7.jpeg" "Alto" => 593 "Ancho" => 900 "Tamanyo" => 92786 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0075" class="elsevierStyleSimplePara elsevierViewall">Pustules, plaques, and ulcerative nodules with erythematous-violaceous coloration, surrounded by a pigmented halo, characteristic of disseminated coccidioidomycosis.</p>" ] ] 7 => array:7 [ "identificador" => "fig0040" "etiqueta" => "Figure 8" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr8.jpeg" "Alto" => 670 "Ancho" => 900 "Tamanyo" => 89789 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0080" class="elsevierStyleSimplePara elsevierViewall">Isolated ulcerated nodule: cutaneous coccidioidomycosis arising from pulmonary dissemination.</p>" ] ] 8 => array:7 [ "identificador" => "fig0045" "etiqueta" => "Figure 9" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr9.jpeg" "Alto" => 1398 "Ancho" => 900 "Tamanyo" => 190290 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0085" class="elsevierStyleSimplePara elsevierViewall">Mature rounded spherules containing multiple endospores of variable size, which are typical structures of <span class="elsevierStyleItalic">Coccidioides</span> species, in infected tissues (hematoxylin-eosin, original magnification<span class="elsevierStyleHsp" style=""></span>×400).</p>" ] ] 9 => array:7 [ "identificador" => "fig0050" "etiqueta" => "Figure 10" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr10.jpeg" "Alto" => 594 "Ancho" => 900 "Tamanyo" => 178307 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0090" class="elsevierStyleSimplePara elsevierViewall">Fungal microorganisms consistent with <span class="elsevierStyleItalic">Coccidioides</span> species in skin biopsy (Gomori-Grocott, original magnification<span class="elsevierStyleHsp" style=""></span>×40).</p>" ] ] 10 => array:7 [ "identificador" => "fig0055" "etiqueta" => "Figure 11" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr11.jpeg" "Alto" => 523 "Ancho" => 900 "Tamanyo" => 69435 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0095" class="elsevierStyleSimplePara elsevierViewall">Nodular lesion 9<span class="elsevierStyleHsp" style=""></span>mm in diameter in a patient with disseminated cryptococcosis and infected with human immunodeficiency virus/AIDS.</p>" ] ] 11 => array:7 [ "identificador" => "fig0060" "etiqueta" => "Figure 12" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr12.jpeg" "Alto" => 1295 "Ancho" => 900 "Tamanyo" => 141688 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0100" class="elsevierStyleSimplePara elsevierViewall">Ulcerated, crusted lesions caused by <span class="elsevierStyleItalic">Cryptococcus neoformans</span> in a hairy area in a patient with AIDS and multiorgan involvement.</p>" ] ] 12 => array:7 [ "identificador" => "fig0065" "etiqueta" => "Figure 13" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr13.jpeg" "Alto" => 620 "Ancho" => 900 "Tamanyo" => 145851 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0105" class="elsevierStyleSimplePara elsevierViewall"><span class="elsevierStyleItalic">Cryptococcus neoformans.</span> India ink staining reveals a thick capsule (original magnification, ×40).</p>" ] ] 13 => array:7 [ "identificador" => "fig0070" "etiqueta" => "Figure 14" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr14.jpeg" "Alto" => 669 "Ancho" => 900 "Tamanyo" => 94194 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0110" class="elsevierStyleSimplePara elsevierViewall">Crusted lesions and umbilicated lesions (different phases of development) caused by <span class="elsevierStyleItalic">Histoplasma capsulatum</span> in a patient with immune reconstitution inflammatory syndrome in different phases of development.</p>" ] ] 14 => array:7 [ "identificador" => "fig0075" "etiqueta" => "Figure 15" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr15.jpeg" "Alto" => 1079 "Ancho" => 1670 "Tamanyo" => 95790 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0115" class="elsevierStyleSimplePara elsevierViewall">Most frequent sites for skin lesions in patients with disseminated histoplasmosis.</p>" ] ] 15 => array:7 [ "identificador" => "tbl0005" "etiqueta" => "Table 1" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "tabla" => array:2 [ "leyenda" => "<p id="spar0125" class="elsevierStyleSimplePara elsevierViewall">Abbreviations: HAART, highly active antiretroviral therapy; HSV, herpes simplex virus; TB, tuberculosis.</p>" "tablatextoimagen" => array:1 [ 0 => array:2 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><thead title="thead"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">Infection \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">Skin/Mucosal Manifestations \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">Differential Diagnosis \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">Treatment \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">Secondary Prophylaxis \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-head\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t" style="border-bottom: 2px solid black">Primary Prophylaxis \t\t\t\t\t\t\n \t\t\t\t</td></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Histoplasmosis \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Skin: papules, pustules, nodules, ulcers, molluscoid lesionsMucosae: oropharynx (vegetative lesions, nodules, ulcers) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Secondary syphilis, prurigo, cryptococcosis, candidiasis, molluscum contagiosum, penicilliosis \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Disseminated disease: Amphotericin B (3 mg/kg/d) for 2 weeks followed by itraconazole (200 mg/twice daily) for 10 weeksIsolated skin lesions: itraconazole 300<span class="elsevierStyleHsp" style=""></span>mg twice daily for 3 days followed by 200 mg/twice daily for 12 weeks \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Itraconazole (200<span class="elsevierStyleHsp" style=""></span>mg twice daily or 400<span class="elsevierStyleHsp" style=""></span>mg once daily) or amphotericin B (50 mg/week); drug indicated for intermittent therapy after 12 months in patients with immune reconstitution with HAART. \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Itraconazole (200 mg/d) in patients living in endemic areas with CD4<span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>150 cells/μL \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Coccidioidomycosis \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Papules, verrucous and/or granulomatous lesions, abscesses, and pustules \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">TB, sporotrichosis, molluscum contagiosum, HSV, rhinophyma, Kaposi sarcoma, and bacterial cellulitis \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Disseminated disease: amphotericin B (0.5–0.7 mg/k/d), for an indeterminate duration \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Fluconazole (400 mg/d) or itraconazole (200<span class="elsevierStyleHsp" style=""></span>mg twice daily), for an indeterminate duration \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Not recommended \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Cryptococcosis \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Papules, pustules, vesicles and/or ulcers, verrucous or necrotic herpetiform, acneiform and varioliform plaques, or even plaques similar to those in Kaposi sarcoma and molluscum contagiosum \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Molluscum contagiosum, herpes simplex, rhinophyma, Kaposi sarcoma, and bacterial cellulitis \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Disseminated disease: Amphotericin B (0.7–1 mg/kg for 7 days) + flucytosine (100 mg/kg for 7 days) for 2 weeks followed by fluconazole (400 mg/d) for 10 weeksIsolated skin lesions: Fluconazole (200–400 mg/d) or itraconazole (400 mg/d) for 2 weeks \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Fluconazole (200–400 mg/d) or itraconazole (400 mg/d), intermittent once immune reconstitution reaches CD4 ><span class="elsevierStyleHsp" style=""></span>10–150 cells/μL for ≥<span class="elsevierStyleHsp" style=""></span>6 months \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Debatable \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab450999.png" ] ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0120" class="elsevierStyleSimplePara elsevierViewall">Treatment and Prophylaxis for Endemic Fungal Infections.</p>" ] ] ] "bibliografia" => array:2 [ "titulo" => "References" "seccion" => array:1 [ 0 => array:2 [ "identificador" => "bibs0005" "bibliografiaReferencia" => array:78 [ 0 => array:3 [ "identificador" => "bib0005" "etiqueta" => "1" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "The morphology of the parasite (histoplasma capsulatum) and the lesions of histoplasmosis, a fatal disease of tropical America" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:1 [ …1] ] ] ] ] "host" => array:1 [ 0 => array:1 [ "Revista" => array:6 [ "tituloSerie" => "J Exp Med" "fecha" => "1909" "volumen" => "11" 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año/Mes | Html | Total | |
---|---|---|---|
2024 Noviembre | 8 | 9 | 17 |
2024 Octubre | 111 | 56 | 167 |
2024 Septiembre | 133 | 54 | 187 |
2024 Agosto | 158 | 133 | 291 |
2024 Julio | 160 | 90 | 250 |
2024 Junio | 158 | 111 | 269 |
2024 Mayo | 143 | 73 | 216 |
2024 Abril | 114 | 47 | 161 |
2024 Marzo | 136 | 61 | 197 |
2024 Febrero | 145 | 59 | 204 |
2024 Enero | 146 | 50 | 196 |
2023 Diciembre | 179 | 43 | 222 |
2023 Noviembre | 240 | 52 | 292 |
2023 Octubre | 229 | 62 | 291 |
2023 Septiembre | 206 | 55 | 261 |
2023 Agosto | 126 | 49 | 175 |
2023 Julio | 126 | 73 | 199 |
2023 Junio | 103 | 38 | 141 |
2023 Mayo | 133 | 54 | 187 |
2023 Abril | 143 | 29 | 172 |
2023 Marzo | 150 | 36 | 186 |
2023 Febrero | 107 | 23 | 130 |
2023 Enero | 108 | 42 | 150 |
2022 Diciembre | 124 | 36 | 160 |
2022 Noviembre | 99 | 39 | 138 |
2022 Octubre | 89 | 20 | 109 |
2022 Septiembre | 142 | 35 | 177 |
2022 Agosto | 135 | 38 | 173 |
2022 Julio | 146 | 46 | 192 |
2022 Junio | 161 | 31 | 192 |
2022 Mayo | 145 | 42 | 187 |
2022 Abril | 162 | 37 | 199 |
2022 Marzo | 115 | 51 | 166 |
2022 Febrero | 118 | 36 | 154 |
2022 Enero | 113 | 61 | 174 |
2021 Diciembre | 59 | 39 | 98 |
2021 Noviembre | 105 | 51 | 156 |
2021 Octubre | 107 | 68 | 175 |
2021 Septiembre | 113 | 91 | 204 |
2021 Agosto | 83 | 39 | 122 |
2021 Julio | 84 | 56 | 140 |
2021 Junio | 92 | 39 | 131 |
2021 Mayo | 98 | 40 | 138 |
2021 Abril | 169 | 62 | 231 |
2021 Marzo | 107 | 27 | 134 |
2021 Febrero | 109 | 34 | 143 |
2021 Enero | 89 | 30 | 119 |
2020 Diciembre | 95 | 27 | 122 |
2020 Noviembre | 45 | 27 | 72 |
2020 Octubre | 41 | 23 | 64 |
2020 Septiembre | 54 | 20 | 74 |
2020 Agosto | 43 | 24 | 67 |
2020 Julio | 52 | 22 | 74 |
2020 Junio | 47 | 41 | 88 |
2020 Mayo | 36 | 23 | 59 |
2020 Abril | 46 | 20 | 66 |
2020 Marzo | 33 | 24 | 57 |
2020 Febrero | 4 | 12 | 16 |
2020 Enero | 4 | 3 | 7 |
2019 Diciembre | 8 | 6 | 14 |
2019 Noviembre | 4 | 5 | 9 |
2019 Octubre | 0 | 4 | 4 |
2019 Septiembre | 8 | 11 | 19 |
2019 Agosto | 4 | 12 | 16 |
2019 Julio | 4 | 19 | 23 |
2019 Junio | 6 | 27 | 33 |
2019 Mayo | 4 | 37 | 41 |
2019 Abril | 2 | 24 | 26 |
2019 Marzo | 2 | 13 | 15 |
2019 Febrero | 2 | 3 | 5 |
2019 Enero | 2 | 7 | 9 |
2018 Diciembre | 2 | 0 | 2 |
2018 Noviembre | 1 | 0 | 1 |
2018 Octubre | 4 | 0 | 4 |
2018 Septiembre | 2 | 0 | 2 |
2018 Marzo | 11 | 1 | 12 |
2018 Febrero | 124 | 10 | 134 |
2018 Enero | 271 | 13 | 284 |
2017 Diciembre | 201 | 13 | 214 |
2017 Noviembre | 147 | 2 | 149 |
2017 Octubre | 127 | 5 | 132 |
2017 Septiembre | 112 | 14 | 126 |
2017 Agosto | 132 | 8 | 140 |
2017 Julio | 123 | 10 | 133 |
2017 Junio | 147 | 20 | 167 |
2017 Mayo | 93 | 21 | 114 |
2017 Abril | 55 | 17 | 72 |
2017 Marzo | 60 | 39 | 99 |
2017 Febrero | 132 | 14 | 146 |
2017 Enero | 105 | 9 | 114 |
2016 Diciembre | 129 | 11 | 140 |
2016 Noviembre | 158 | 18 | 176 |
2016 Octubre | 213 | 27 | 240 |
2016 Septiembre | 236 | 14 | 250 |
2016 Agosto | 281 | 23 | 304 |
2016 Julio | 130 | 12 | 142 |
2016 Junio | 14 | 12 | 26 |
2016 Mayo | 19 | 17 | 36 |
2016 Abril | 17 | 4 | 21 |
2016 Marzo | 17 | 5 | 22 |
2016 Febrero | 17 | 4 | 21 |
2016 Enero | 10 | 3 | 13 |
2015 Diciembre | 11 | 3 | 14 |
2015 Noviembre | 8 | 9 | 17 |
2015 Octubre | 10 | 3 | 13 |
2015 Septiembre | 8 | 12 | 20 |
2015 Agosto | 10 | 9 | 19 |
2015 Julio | 219 | 16 | 235 |
2015 Junio | 170 | 13 | 183 |
2015 Mayo | 170 | 12 | 182 |
2015 Abril | 138 | 11 | 149 |
2015 Marzo | 190 | 3 | 193 |
2015 Febrero | 176 | 4 | 180 |
2015 Enero | 123 | 3 | 126 |
2014 Diciembre | 103 | 13 | 116 |
2014 Noviembre | 134 | 3 | 137 |
2014 Octubre | 129 | 2 | 131 |
2014 Septiembre | 127 | 4 | 131 |
2014 Agosto | 111 | 6 | 117 |
2014 Julio | 94 | 6 | 100 |
2014 Junio | 90 | 5 | 95 |
2014 Mayo | 91 | 12 | 103 |
2014 Abril | 80 | 8 | 88 |
2014 Marzo | 67 | 11 | 78 |
2014 Febrero | 22 | 13 | 35 |
2014 Enero | 0 | 5 | 5 |