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array:25 [ "pii" => "S1578219020300317" "issn" => "15782190" "doi" => "10.1016/j.adengl.2020.03.007" "estado" => "S300" "fechaPublicacion" => "2020-04-01" "aid" => "2226" "copyright" => "AEDV" "copyrightAnyo" => "2019" "documento" => "article" "crossmark" => 1 "licencia" => "http://creativecommons.org/licenses/by-nc-nd/4.0/" "subdocumento" => "rev" "cita" => "Actas Dermosifiliogr. 2020;111:196-204" "abierto" => array:3 [ "ES" => true "ES2" => true "LATM" => true ] "gratuito" => true "lecturas" => array:1 [ "total" => 0 ] "Traduccion" => array:1 [ "es" => array:20 [ "pii" => "S0001731019301917" "issn" => "00017310" "doi" => "10.1016/j.ad.2019.02.013" "estado" => "S300" "fechaPublicacion" => "2020-04-01" "aid" => "2226" "copyright" => "AEDV" "documento" => "article" "crossmark" => 1 "licencia" => "http://creativecommons.org/licenses/by-nc-nd/4.0/" "subdocumento" => "rev" "cita" => "Actas Dermosifiliogr. 2020;111:196-204" "abierto" => array:3 [ "ES" => true "ES2" => true "LATM" => true ] "gratuito" => true "lecturas" => array:2 [ "total" => 86 "formatos" => array:2 [ "HTML" => 53 "PDF" => 33 ] ] "es" => array:14 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">REVISIÓN</span>" "titulo" => "Dermatosis purpúricas pigmentadas. 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"apellidos" => "Martínez Pallás" ] 1 => array:2 [ "nombre" => "R." "apellidos" => "Conejero del Mazo" ] 2 => array:2 [ "nombre" => "V." "apellidos" => "Lezcano Biosca" ] ] ] ] "resumen" => array:1 [ 0 => array:3 [ "titulo" => "Graphical abstract" "clase" => "graphical" "resumen" => "<span id="abst0005" class="elsevierStyleSection elsevierViewall"><p id="spar0005" class="elsevierStyleSimplePara elsevierViewall"><elsevierMultimedia ident="fig0045"></elsevierMultimedia></p></span>" ] ] ] "idiomaDefecto" => "es" "Traduccion" => array:1 [ "en" => array:9 [ "pii" => "S1578219020300317" "doi" => "10.1016/j.adengl.2020.03.007" "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/S1578219020300317?idApp=UINPBA000044" ] ] "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S0001731019301917?idApp=UINPBA000044" "url" => "/00017310/0000011100000003/v3_202009190646/S0001731019301917/v3_202009190646/es/main.assets" ] ] "itemSiguiente" => array:20 [ "pii" => "S1578219020300238" "issn" => "15782190" "doi" => "10.1016/j.adengl.2020.03.001" "estado" => "S300" "fechaPublicacion" => "2020-04-01" "aid" => "2287" "copyright" => "AEDV" "documento" => "article" "crossmark" => 1 "licencia" => "http://creativecommons.org/licenses/by-nc-nd/4.0/" "subdocumento" => "rev" "cita" => "Actas Dermosifiliogr. 2020;111:205-21" "abierto" => array:3 [ "ES" => true "ES2" => true "LATM" => true ] "gratuito" => true "lecturas" => array:1 [ "total" => 0 ] "en" => array:13 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Review</span>" "titulo" => "Innovation in Atopic Dermatitis: From Pathogenesis to Treatment" "tienePdf" => "en" "tieneTextoCompleto" => "en" "tieneResumen" => array:2 [ 0 => "en" 1 => "es" ] "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "205" "paginaFinal" => "221" ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Innovación en dermatitis atópica: de la patogenia a la terapéutica" ] ] "contieneResumen" => array:2 [ "en" => true "es" => true ] "contieneTextoCompleto" => array:1 [ "en" => true ] "contienePdf" => array:1 [ "en" => true ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:8 [ "identificador" => "fig0005" "etiqueta" => "Figure 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 1641 "Ancho" => 2925 "Tamanyo" => 443688 ] ] "detalles" => array:1 [ 0 => array:3 [ "identificador" => "at0005" "detalle" => "Figure " "rol" => "short" ] ] "descripcion" => array:1 [ "en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Biologic agents and specific targets in the pathogenesis of atopic dermatitis.</p> <p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">Abbreviations: IgE, immunoglobulin E; IL, interleukin; OSMRß; oncostatin M receptor ß; Th, T helper (lymphocyte); TSLP, thymic stromal lymphopoietin.</p>" ] ] ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "M. Munera-Campos, J.M. Carrascosa" "autores" => array:2 [ 0 => array:2 [ "nombre" => "M." "apellidos" => "Munera-Campos" ] 1 => array:2 [ "nombre" => "J.M." "apellidos" => "Carrascosa" ] ] ] ] ] "idiomaDefecto" => "en" "Traduccion" => array:1 [ "es" => array:9 [ "pii" => "S0001731019303898" "doi" => "10.1016/j.ad.2019.11.002" "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/S0001731019303898?idApp=UINPBA000044" ] ] "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S1578219020300238?idApp=UINPBA000044" "url" => "/15782190/0000011100000003/v1_202005050702/S1578219020300238/v1_202005050702/en/main.assets" ] "itemAnterior" => array:20 [ "pii" => "S1578219020300287" "issn" => "15782190" "doi" => "10.1016/j.adengl.2020.03.005" "estado" => "S300" "fechaPublicacion" => "2020-04-01" "aid" => "2291" "copyright" => "AEDV" "documento" => "article" "crossmark" => 1 "licencia" => "http://creativecommons.org/licenses/by-nc-nd/4.0/" "subdocumento" => "sco" "cita" => "Actas Dermosifiliogr. 2020;111:192-5" "abierto" => array:3 [ "ES" => true "ES2" => true "LATM" => true ] "gratuito" => true "lecturas" => array:1 [ "total" => 0 ] "en" => array:11 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Opinion Article</span>" "titulo" => "Deep Learning and Mathematical Models in Dermatology" "tienePdf" => "en" "tieneTextoCompleto" => "en" "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "192" "paginaFinal" => "195" ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "<span class="elsevierStyleItalic">Deep learning</span> y DerMATología" ] ] "contieneTextoCompleto" => array:1 [ "en" => true ] "contienePdf" => array:1 [ "en" => true ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:8 [ "identificador" => "fig0010" "etiqueta" => "Fig. 2" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr2.jpeg" "Alto" => 2238 "Ancho" => 2508 "Tamanyo" => 346979 ] ] "detalles" => array:1 [ 0 => array:3 [ "identificador" => "at0025" "detalle" => "Fig. " "rol" => "short" ] ] "descripcion" => array:1 [ "en" => "<p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">A, Example of a convolution operation. A computer sees an image (L) as a 4<span class="elsevierStyleHsp" style=""></span>×<span class="elsevierStyleHsp" style=""></span>4 matrix of numbers. Each value of the input image is multiplied by a filter or kernel. Consequently, a new, reduced representation is obtained (a 2<span class="elsevierStyleHsp" style=""></span>×<span class="elsevierStyleHsp" style=""></span>2 feature map). B, Example of a specific operation for the values in the blue box.</p>" ] ] ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "Á. Iglesias-Puzas, P. Boixeda" "autores" => array:2 [ 0 => array:2 [ "nombre" => "Á." "apellidos" => "Iglesias-Puzas" ] 1 => array:2 [ "nombre" => "P." "apellidos" => "Boixeda" ] ] ] ] ] "idiomaDefecto" => "en" "Traduccion" => array:1 [ "es" => array:9 [ "pii" => "S000173101930393X" "doi" => "10.1016/j.ad.2019.01.014" "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/S000173101930393X?idApp=UINPBA000044" ] ] "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S1578219020300287?idApp=UINPBA000044" "url" => "/15782190/0000011100000003/v1_202005050702/S1578219020300287/v1_202005050702/en/main.assets" ] "en" => array:21 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Review</span>" "titulo" => "Pigmented Purpuric Dermatosis: A Review of the Literature" "tieneTextoCompleto" => true "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "196" "paginaFinal" => "204" ] ] "autores" => array:1 [ 0 => array:4 [ "autoresLista" => "I. Martínez Pallás, R. Conejero del Mazo, V. Lezcano Biosca" "autores" => array:3 [ 0 => array:4 [ "nombre" => "I." "apellidos" => "Martínez Pallás" "email" => array:1 [ 0 => "isabel_mp91@hotmail.com" ] "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "*" "identificador" => "cor0005" ] ] ] 1 => array:2 [ "nombre" => "R." "apellidos" => "Conejero del Mazo" ] 2 => array:2 [ "nombre" => "V." "apellidos" => "Lezcano Biosca" ] ] "afiliaciones" => array:1 [ 0 => array:2 [ "entidad" => "Servicio de Dermatología y Venereología, Hospital Clínico Lozano Blesa, Zaragoza, Spain" "identificador" => "aff0005" ] ] "correspondencia" => array:1 [ 0 => array:3 [ "identificador" => "cor0005" "etiqueta" => "⁎" "correspondencia" => "Corresponding author." ] ] ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Dermatosis purpúricas pigmentadas. Revisión de la literatura científica" ] ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:8 [ "identificador" => "fig0020" "etiqueta" => "Figure 4" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr4.jpeg" "Alto" => 680 "Ancho" => 904 "Tamanyo" => 76759 ] ] "detalles" => array:1 [ 0 => array:3 [ "identificador" => "at0020" "detalle" => "Figure " "rol" => "short" ] ] "descripcion" => array:1 [ "en" => "<p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">Majocchi disease. Annular red-violaceous lesions on the leg.</p>" ] ] ] "textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Introduction</span><p id="par0005" class="elsevierStylePara elsevierViewall">The pigmented purpuric dermatoses (PPDs) are a rare group of chronic, benign diseases characterized by multiple petechiae on hyperpigmented, yellowish-brown macules.<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> The different variants are distinct clinical forms of the same entity with similar histopathologic features.<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2,3</span></a></p><p id="par0010" class="elsevierStylePara elsevierViewall">There are 5 classic variants: Schamberg disease (progressive PPD), eczematoid purpura of Doucas and Kapetanakis (pruritic purpura), pigmented purpuric lichenoid dermatosis of Gougerot and Blum, lichen aureus (lichen purpuricus), and Majocchi disease (purpura annularis telangiectodes).<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> Less common variants are granulomatous PPD, itching purpura of Loewenthal, linear PPD, transitory PPD, and familial PPD.<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a></p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Epidemiology</span><p id="par0015" class="elsevierStylePara elsevierViewall">PPDs are rare and predominantly affect adults,<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> although cases have been reported in children.<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a> The most common variant in both adults and children is Schamberg disease. PPDs, and linear forms in particular,<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">6</span></a> are generally more common in men.<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> Majocchi disease is more common in women.</p></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Etiology and Pathogenesis</span><p id="par0020" class="elsevierStylePara elsevierViewall">Although the causes of the PPDs are unknown, a range of triggering factors have been proposed, including exercise, venous hypertension, diabetes mellitus, infections,<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2,7</span></a> and various medications (<a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>).<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">8</span></a> An association with dyslipidemia and autoimmune diseases has been reported for granulomatous PPD.<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">9</span></a> In most cases, however, no cause is identified.<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">10</span></a></p><elsevierMultimedia ident="tbl0005"></elsevierMultimedia><p id="par0025" class="elsevierStylePara elsevierViewall">Capillary dilation and fragility have been attributed a possible pathogenic role in PPDs.<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">10</span></a> It has been hypothesized that the cells responsible for these disorders are cells involved in blood vessel structure, such as fibroblasts and endothelial cells. Whether through activation (e.g., high intravascular pressure) or spontaneously, the function of these cells may be altered, causing red blood cells (RBCs) to leak through the vessel walls,<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">11</span></a> triggering a cell-mediated hypersensitivity reaction. Cell-mediated immune response would therefore appear to have a fundamental role in the pathogenesis of PPDs.<a class="elsevierStyleCrossRefs" href="#bib0060"><span class="elsevierStyleSup">12,13</span></a> The perivascular inflammatory infiltrate is made up of CD4<span class="elsevierStyleSup">+</span> T cells<a class="elsevierStyleCrossRef" href="#bib0070"><span class="elsevierStyleSup">14</span></a> (with reduced CD7 expression<a class="elsevierStyleCrossRef" href="#bib0075"><span class="elsevierStyleSup">15</span></a>) and CD1a<span class="elsevierStyleSup">+</span> dendritic cells.<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">12</span></a></p><p id="par0030" class="elsevierStylePara elsevierViewall">The pathogenic role of cell adhesion molecules in PPDs has also been analyzed in several studies. CAMs are membrane proteins that interact with specific ligands that provide and maintain contact between different cells and between cells and extracellular matrix proteins. High expression levels have been observed for adhesion molecules LFA-1 (lymphocyte function antigen-1) and ICAM-1 (intercellular adhesion molecule-1) in inflammatory cells and for ICAM-1 and ELAM-1 (endothelial leukocyte adhesion molecule- 1)<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">12</span></a> in endothelial cells. T cells activated by an antigenic stimulus would thus adhere to endothelial cells, fibroblasts, and keratinocytes.<a class="elsevierStyleCrossRef" href="#bib0080"><span class="elsevierStyleSup">16</span></a> Cytokines produced by leukocytes (e.g., tumor necrosis factor α) can trigger the expression of these adhesion molecules (<a class="elsevierStyleCrossRef" href="#fig0005">Fig. 1</a>).</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0035" class="elsevierStylePara elsevierViewall">The above cytokines may also result in a decreased release of the endothelial plasminogen activator and/or an excessive increase in the plasminogen activator inhibitor,<a class="elsevierStyleCrossRef" href="#bib0085"><span class="elsevierStyleSup">17</span></a> leading to the reduced fibrinolytic activity and intraperivascular deposition of fibrin observed in PPDs.<a class="elsevierStyleCrossRef" href="#bib0090"><span class="elsevierStyleSup">18</span></a></p><p id="par0040" class="elsevierStylePara elsevierViewall">Direct immunofluorescence may show fibrinogen, immunoglobulin M, and/or C3 deposition in the superficial dermal vessels.<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">10</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">Another hypothesis that has emerged in recent years is that PPDs may represent an insidious epitheliotropic T-cell alteration. This theory is supported by the observation of epidermotropism or a monoclonal pattern in the inflammatory infiltrate.<a class="elsevierStyleCrossRefs" href="#bib0075"><span class="elsevierStyleSup">15,19</span></a> There have even been some reports of progression to mycosis fungoides.<a class="elsevierStyleCrossRefs" href="#bib0100"><span class="elsevierStyleSup">20–22</span></a> As it is difficult to distinguish between purpuric mycosis fungoides and monoclonal PPD, it is essential to integrate clinical, molecular, and histopathologic findings.<a class="elsevierStyleCrossRefs" href="#bib0075"><span class="elsevierStyleSup">15,20,23</span></a> Poikiloderma, pruritus, coalescing plaques, a duration of more than 1 year, a monoclonal pattern, and decreased CD7 and CD62 L expression in the infiltrate should all raise suspicion of disease progression, even in the absence of overt lymphocytic atypia.<a class="elsevierStyleCrossRefs" href="#bib0075"><span class="elsevierStyleSup">15,24</span></a> Some authors opt to treat disseminated and monoclonal DPP as early-stage mycosis fungoides.</p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0040">Clinical Variants</span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0045">Progressive PPD or Schamberg Disease<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1,2</span></a></span><p id="par0050" class="elsevierStylePara elsevierViewall">In progressive PPD or Schamberg disease, lesions usually appear on both lower extremities, but they can also affect the trunk, arms, thighs, or buttocks. They present as orange-red macules with peripheral purpuric spots resembling grains of cayenne pepper (<a class="elsevierStyleCrossRef" href="#fig0010">Fig. 2</a>A and B); these spots acquire a yellowish-brown color as they progress. The lesions are generally asymptomatic, although some patients describe pruritus. They follow a chronic course with numerous relapses and remissions.</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0050">Pruritic Purpura or Eczematoid Purpura of Doucas And Kapetanakis<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1,25</span></a></span><p id="par0055" class="elsevierStylePara elsevierViewall">Pruritic purpura or eczematoid purpura of Doucas and Kapetanakis is the most extensive and pruritic variant of the PPDs. It mostly affects the lower extremities and is clinically similar to Schamberg disease, with purpuric or petechial macules but with a scaling surface. Eczematoid purpura of Doucas and Kapetanakis has been associated with allergic contact dermatitis to rubber and clothing. Onset is rapid (15–30 days) and the lesions can last for months or years.</p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0055">Pigmented Purpuric Lichenoid Dermatosis of Gougerot and Blum<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1,2,26</span></a></span><p id="par0060" class="elsevierStylePara elsevierViewall">Lichenoid pigmented purpuric dermatosis of Gougerot and Blum is characterized by violaceous lichenoid papules that tend to merge, forming large plaques that are usually located on the legs but may affect the trunk. The condition follows a chronic course and usually affects elderly men. It should be distinguished from Kaposi sarcoma.</p></span><span id="sec0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0060">Lichen Aureus or Lichen Purpuricus<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1,2,27</span></a></span><p id="par0065" class="elsevierStylePara elsevierViewall">Lichen aureus or lichen purpuricus is a more localized variant of PPD. Lesions are persistent and are typically solitary or small in number. Lichen aureus is characterized by the sudden appearance of small yellow-orangish papules with a lichenoid appearance and a tendency to coalesce into plaques measuring between 1 and 20 cm associated with millimetric purpuric lesions (<a class="elsevierStyleCrossRef" href="#fig0015">Fig. 3</a>). The condition mostly affects the lower extremities, but lesions can occur on any part of the body. They are usually asymptomatic. Zosteriform<a class="elsevierStyleCrossRef" href="#bib0140"><span class="elsevierStyleSup">28</span></a> and segmental variants along the lines of Blaschko<a class="elsevierStyleCrossRef" href="#bib0145"><span class="elsevierStyleSup">29</span></a> or following the course of the saphenous<a class="elsevierStyleCrossRef" href="#bib0150"><span class="elsevierStyleSup">30</span></a> or cephalic veins<a class="elsevierStyleCrossRef" href="#bib0155"><span class="elsevierStyleSup">31</span></a> have been described in children and adolescents.</p><elsevierMultimedia ident="fig0015"></elsevierMultimedia></span><span id="sec0045" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0065">Purpura Annularis Telangiectodes or Majocchi Disease<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1,2,25</span></a></span><p id="par0070" class="elsevierStylePara elsevierViewall">Purpura annularis telangiectodes or Majocchi disease presents with annular red-violaceous macules (<a class="elsevierStyleCrossRef" href="#fig0020">Fig. 4</a>), followed by darker red telangiectatic puncta. The lesions extend peripherally and their center gradually fades and may acquire an atrophic appearance. The eruption begins in the lower extremities and then spreads to the trunk and arms; it is characterized by large numbers of lesions. A variant known as <span class="elsevierStyleItalic">arciform purpura annularis telangiectodes</span> featuring fewer but larger lesions with a characteristic arched morphology has been described.<a class="elsevierStyleCrossRef" href="#bib0160"><span class="elsevierStyleSup">32</span></a></p><elsevierMultimedia ident="fig0020"></elsevierMultimedia></span><span id="sec0050" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0070">Other Variants</span><p id="par0075" class="elsevierStylePara elsevierViewall">Hersch and Schwayder<a class="elsevierStyleCrossRef" href="#bib0165"><span class="elsevierStyleSup">33</span></a> described what is considered to be a rare linear, unilateral form that must be differentiated from linear forms of Schamberg disease and lichen aureus. Higgins and Cox<a class="elsevierStyleCrossRef" href="#bib0170"><span class="elsevierStyleSup">34</span></a> described a quadrantic form they attributed to a vascular obstruction in the pelvis.</p><p id="par0080" class="elsevierStylePara elsevierViewall">There have also been reports of a transitory variant<a class="elsevierStyleCrossRef" href="#bib0175"><span class="elsevierStyleSup">35</span></a> including entities such as angioma serpiginosum,<a class="elsevierStyleCrossRef" href="#bib0180"><span class="elsevierStyleSup">36</span></a> which is an uncommon vascular disorder that usually begins in childhood, is more common in females, and shows evidence of estrogen dependence. Angioma serpiginosum is characterized by multiple asymptomatic red-purpuric macules arranged in small groups following a serpiginosum pattern along the extremities.</p><p id="par0085" class="elsevierStylePara elsevierViewall">Itching purpura of Loewenthal,<a class="elsevierStyleCrossRef" href="#bib0185"><span class="elsevierStyleSup">37</span></a> which has only been described in adults, is considered a more symptomatic variant of Schamberg disease.</p><p id="par0090" class="elsevierStylePara elsevierViewall">Granulomatous PPD, described by Saito,<a class="elsevierStyleCrossRef" href="#bib0190"><span class="elsevierStyleSup">38</span></a> is a histopathologic form that is more common in women and is clinically indistinguishable from other DPPs.</p><p id="par0095" class="elsevierStylePara elsevierViewall">Finally, there have been reports of autosomal dominant familial forms of Schamberg disease and purpura annularis telangiectoides.<a class="elsevierStyleCrossRef" href="#bib0195"><span class="elsevierStyleSup">39</span></a></p></span></span><span id="sec0055" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0075">Histopathology</span><p id="par0100" class="elsevierStylePara elsevierViewall">Histopathologically, PPDs are characterized by a perivascular lymphocytic infiltrate centered on the superficial small vessels. Other typical findings are endothelial swelling, luminal narrowing,<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">10</span></a> extravasated RBCs, and hemosiderin-laden macrophages (<a class="elsevierStyleCrossRef" href="#fig0025">Fig. 5</a> A and B). Perls and Fontana-Masson staining shows hemosiderin (iron) deposits in the superficial dermis, setting DPP apart from stasis dermatitis, which has deeper deposits.<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a></p><elsevierMultimedia ident="fig0025"></elsevierMultimedia><p id="par0105" class="elsevierStylePara elsevierViewall">A characteristic finding of lichen aureus is an intact epidermis separated from a band-like dermal infiltrate by an area of spared connective tissue (Grenz area)<a class="elsevierStyleCrossRef" href="#bib0135"><span class="elsevierStyleSup">27</span></a> (<a class="elsevierStyleCrossRef" href="#fig0030">Fig. 6</a>). This infiltrate is also typical in pigmented purpuric lichenoid dermatosis of Gougerot and Blum.<a class="elsevierStyleCrossRef" href="#bib0130"><span class="elsevierStyleSup">26</span></a> Eczematoid purpura of Doucas and Kapetanakis, by contrast, features epidermal spongiosis and neutrophils in the infiltrate.<a class="elsevierStyleCrossRef" href="#bib0125"><span class="elsevierStyleSup">25</span></a> Granulomatous PPD is characterized by a perivascular granulomatous infiltrate overlying typical features.<a class="elsevierStyleCrossRef" href="#bib0190"><span class="elsevierStyleSup">38</span></a> A comparison of clinical features, location, and histopathologic findings for the most common variants of PPD is provided in <a class="elsevierStyleCrossRef" href="#tbl0010">Table 2</a>.</p><elsevierMultimedia ident="fig0030"></elsevierMultimedia><elsevierMultimedia ident="tbl0010"></elsevierMultimedia><p id="par0110" class="elsevierStylePara elsevierViewall">While some authors<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1,13</span></a> consider capillaritis to be a defining feature of DPPs, Ackerman<a class="elsevierStyleCrossRef" href="#bib0200"><span class="elsevierStyleSup">40</span></a> does not believe this to be the case as there is an absence of fibrin in the luminal wall and thrombi in the lumina.</p></span><span id="sec0060" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0080">Diagnosis</span><p id="par0115" class="elsevierStylePara elsevierViewall">In addition to skin biopsy, a blood test is recommended to rule out thrombocytopenia, clotting or autoimmune disorders (antinuclear antibodies, rheumatoid factor), and chronic infections (anti-HCV and anti-HBsAg).<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a></p><span id="sec0065" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0085">Differential Diagnosis</span><p id="par0120" class="elsevierStylePara elsevierViewall">The differential diagnosis should include other conditions featuring purpuric manifestations involving the lower extremities. These entities and their main characteristics are summarized in <a class="elsevierStyleCrossRef" href="#tbl0015">Table 3</a>.</p><elsevierMultimedia ident="tbl0015"></elsevierMultimedia></span><span id="sec0070" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0090">Dermoscopy</span><p id="par0125" class="elsevierStylePara elsevierViewall">The most common dermoscopic finding is a diffuse coppery-red background that histopathologically corresponds to the lymphocytic dermal infiltrate, extravasated RBCs, and hemosiderin-laden macrophages.<a class="elsevierStyleCrossRef" href="#bib0205"><span class="elsevierStyleSup">41</span></a> Other findings include red globules and dots, which can be explained by the extravasated RBCs, the increased number of blood vessels, and the dilation of these vessels<a class="elsevierStyleCrossRef" href="#bib0210"><span class="elsevierStyleSup">42</span></a> (<a class="elsevierStyleCrossRef" href="#fig0035">Fig. 7</a>). Brown dots are observed in almost 50% of patients and correspond to the spherical or elliptical arrangement of melanocytes and melanophages at the dermoepidermal junction. In a third of cases, dermoscopy shows a pigmented pseudo-network that corresponds to the hyperpigmented basal cell layer and incontinentia pigmenti in the papillary dermis. Specific dermoscopic findings reported for lichen aureus include a coppery-red background with brown and red dots and globules, gray dots, and a pseudo-network comprising interconnected pigmented lines<a class="elsevierStyleCrossRef" href="#bib0215"><span class="elsevierStyleSup">43</span></a> (<a class="elsevierStyleCrossRef" href="#fig0040">Fig. 8</a>).</p><elsevierMultimedia ident="fig0035"></elsevierMultimedia><elsevierMultimedia ident="fig0040"></elsevierMultimedia></span></span><span id="sec0075" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0095">Treatment</span><p id="par0130" class="elsevierStylePara elsevierViewall">Considering that DPPs are benign and no standardized treatments with proven effectiveness exist, the risks and benefits of any treatment should be carefully weighed up.</p><p id="par0135" class="elsevierStylePara elsevierViewall">Due to the benign, largely asymptomatic nature of the DPPs, no treatment is an option.<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a> Treatment, however, is often called for because of the chronic nature of the disease, its physical and psychological impacts, and the presence of extensive lesions or itching.</p><p id="par0140" class="elsevierStylePara elsevierViewall">Most of the treatment recommendations are based on small case series, and none of them are backed by sufficient evidence to be considered a universal treatment.</p><p id="par0145" class="elsevierStylePara elsevierViewall">A range of topical and systemic treatments, detailed below, have been described in small series and case reports.</p><span id="sec0080" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0100">Topical Treatments</span><span id="sec0085" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0105">Topical Corticosteroids</span><p id="par0150" class="elsevierStylePara elsevierViewall">Topical corticosteroids are the most common treatments described and have been observed to reduce itching and in some cases clear lesions.<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2,4</span></a></p><p id="par0155" class="elsevierStylePara elsevierViewall">The most widely used agents are medium- and high-potency corticosteroids (clobetasol and methylprednisolone aceponate)</p></span><span id="sec0090" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0110">Topical Calcineurin Inhibitors</span><p id="par0160" class="elsevierStylePara elsevierViewall">Topical application of tacrolimus<a class="elsevierStyleCrossRef" href="#bib0220"><span class="elsevierStyleSup">44</span></a> and pimecrolimus<a class="elsevierStyleCrossRef" href="#bib0225"><span class="elsevierStyleSup">45</span></a> for several months has been found to resolve lichen aureus.</p><p id="par0165" class="elsevierStylePara elsevierViewall">Given the chronic nature of PPD lesions and the need for long-term treatment, calcineurin inhibitors can be considered a good alternative to topical corticosteroids for clearing or resolving lesions.</p></span></span><span id="sec0095" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0115">Phototherapy</span><p id="par0170" class="elsevierStylePara elsevierViewall">Phototherapy is a good option for treating extensive disease or PPD that does not respond to topical corticosteroids or calcineurin inhibitors.</p><p id="par0175" class="elsevierStylePara elsevierViewall">It has been postulated that phototherapy may be effective because it produces an immunomodulatory effect that modifies T-cell activity and reduces the production of interleukin 2, resulting in improvement.<a class="elsevierStyleCrossRef" href="#bib0230"><span class="elsevierStyleSup">46</span></a></p><p id="par0180" class="elsevierStylePara elsevierViewall">Psoralen and UV-A (PUVA) treatment has been used successfully in patients with Schamberg disease, lichenoid purpuric dermatosis, and lichen aureus. In the series published to date, between 7 and 29 sessions with cumulative doses ranging from 16 to 49 J/cm<span class="elsevierStyleSup">2</span> have been needed to achieve remission. Retreatment has also proven effective, and in some cases maintenance treatment over several months has been necessary to prolong response.<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2,47–49</span></a></p><p id="par0185" class="elsevierStylePara elsevierViewall">Narrowband UV-B phototherapy with cumulative doses of between 11 and 49 J/cm<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a> administered in 24 to 60 sessions has produced favorable responses in patients with different clinical variants of DPP. As with PUVA treatment, there have been reports of recurrence after treatment discontinuation but good response to retreatment.<a class="elsevierStyleCrossRefs" href="#bib0230"><span class="elsevierStyleSup">46,50,51</span></a></p><p id="par0190" class="elsevierStylePara elsevierViewall">Narrowband UV-B therapy is considered to be a good option because of its few adverse effects and good tolerability profile. It should therefore be borne in mind as an option for pediatric patients, patients with extensive lesions, and patients resistant to topical treatments.<a class="elsevierStyleCrossRefs" href="#bib0025"><span class="elsevierStyleSup">5,52</span></a></p></span><span id="sec0100" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0120">Systemic Treatments</span><span id="sec0105" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0125">Pentoxifylline</span><p id="par0195" class="elsevierStylePara elsevierViewall">There have been reports of PPD responding to oral pentoxifylline. It has been suggested that pentoxifylline may be effective because it inhibits T-cell adherence to the vascular endothelium by interaction with ICAM-1.<a class="elsevierStyleCrossRefs" href="#bib0265"><span class="elsevierStyleSup">53,54</span></a></p><p id="par0200" class="elsevierStylePara elsevierViewall">Pentoxifylline has been used alone, at a dose of 400 mg twice or three times daily for 2 to 3 months,<a class="elsevierStyleCrossRefs" href="#bib0210"><span class="elsevierStyleSup">42,43</span></a> or in combination with other drugs such as prostacyclins (prostaglandin I1)<a class="elsevierStyleCrossRef" href="#bib0275"><span class="elsevierStyleSup">55</span></a> and oral corticosteroids.<a class="elsevierStyleCrossRef" href="#bib0280"><span class="elsevierStyleSup">56</span></a> Pentoxifylline has also been found to be ineffective in the treatment of DPPs.<a class="elsevierStyleCrossRef" href="#bib0285"><span class="elsevierStyleSup">57</span></a></p></span><span id="sec0110" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0130">Ascorbic Acid and Bioflavonoids (Rutin/Rutoside)</span><p id="par0205" class="elsevierStylePara elsevierViewall">As ascorbic acid and bioflavonoids increase collagen production, thereby reducing vascular permeability and improving the vascular endothelial barrier function, high doses of vitamin C combined with a flavonoid glycoside (like rutoside/rutin), present in citrus fruits, administered over several months have resulted in clinical improvements and in some cases resolution.<a class="elsevierStyleCrossRef" href="#bib0290"><span class="elsevierStyleSup">58</span></a></p></span></span><span id="sec0115" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0135">Other Treatments</span><p id="par0210" class="elsevierStylePara elsevierViewall">There have been isolated reports of response to various systemic treatments, such as griseofulvin,<a class="elsevierStyleCrossRef" href="#bib0295"><span class="elsevierStyleSup">59</span></a> colchicine,<a class="elsevierStyleCrossRef" href="#bib0300"><span class="elsevierStyleSup">60</span></a> methotrexate,<a class="elsevierStyleCrossRef" href="#bib0305"><span class="elsevierStyleSup">61</span></a> and ciclosporin.<a class="elsevierStyleCrossRef" href="#bib0310"><span class="elsevierStyleSup">62</span></a></p></span></span><span id="sec0120" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0140">Conclusions</span><p id="par0215" class="elsevierStylePara elsevierViewall">The DPPs are a common dermatological condition and have a major impact on patient quality of life due to both symptoms and cosmetic concerns. Although the different variants are clinically very similar, there are a number of clinical, histopathologic, and dermoscopic characteristics that help to establish a more specific diagnosis.</p><p id="par0220" class="elsevierStylePara elsevierViewall">Finally, while there is insufficient evidence in the literature to recommend any treatment as a first-line treatment, numerous options exist that can achieve considerable improvements.</p></span><span id="sec0125" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0145">Conflicts of Interest</span><p id="par0225" class="elsevierStylePara elsevierViewall">The authors declare that they have no conflicts of interest.</p></span></span>" "textoCompletoSecciones" => array:1 [ "secciones" => array:15 [ 0 => array:3 [ "identificador" => "xres1332886" "titulo" => "Abstract" "secciones" => array:1 [ 0 => array:1 [ "identificador" => "abst0005" ] ] ] 1 => array:2 [ "identificador" => "xpalclavsec1227991" "titulo" => "Keywords" ] 2 => array:3 [ "identificador" => "xres1332885" "titulo" => "Resumen" "secciones" => array:1 [ 0 => array:1 [ "identificador" => "abst0010" ] ] ] 3 => array:2 [ "identificador" => "xpalclavsec1227992" "titulo" => "Palabras clave" ] 4 => array:2 [ "identificador" => "sec0005" "titulo" => "Introduction" ] 5 => array:2 [ "identificador" => "sec0010" "titulo" => "Epidemiology" ] 6 => array:2 [ "identificador" => "sec0015" "titulo" => "Etiology and Pathogenesis" ] 7 => array:3 [ "identificador" => "sec0020" "titulo" => "Clinical Variants" "secciones" => array:6 [ 0 => array:2 [ "identificador" => "sec0025" "titulo" => "Progressive PPD or Schamberg Disease" ] 1 => array:2 [ "identificador" => "sec0030" "titulo" => "Pruritic Purpura or Eczematoid Purpura of Doucas And Kapetanakis" ] 2 => array:2 [ "identificador" => "sec0035" "titulo" => "Pigmented Purpuric Lichenoid Dermatosis of Gougerot and Blum" ] 3 => array:2 [ "identificador" => "sec0040" "titulo" => "Lichen Aureus or Lichen Purpuricus" ] 4 => array:2 [ "identificador" => "sec0045" "titulo" => "Purpura Annularis Telangiectodes or Majocchi Disease" ] 5 => array:2 [ "identificador" => "sec0050" "titulo" => "Other Variants" ] ] ] 8 => array:2 [ "identificador" => "sec0055" "titulo" => "Histopathology" ] 9 => array:3 [ "identificador" => "sec0060" "titulo" => "Diagnosis" "secciones" => array:2 [ 0 => array:2 [ "identificador" => "sec0065" "titulo" => "Differential Diagnosis" ] 1 => array:2 [ "identificador" => "sec0070" "titulo" => "Dermoscopy" ] ] ] 10 => array:3 [ "identificador" => "sec0075" "titulo" => "Treatment" "secciones" => array:4 [ 0 => array:3 [ "identificador" => "sec0080" "titulo" => "Topical Treatments" "secciones" => array:2 [ 0 => array:2 [ "identificador" => "sec0085" "titulo" => "Topical Corticosteroids" ] 1 => array:2 [ "identificador" => "sec0090" "titulo" => "Topical Calcineurin Inhibitors" ] ] ] 1 => array:2 [ "identificador" => "sec0095" "titulo" => "Phototherapy" ] 2 => array:3 [ "identificador" => "sec0100" "titulo" => "Systemic Treatments" "secciones" => array:2 [ 0 => array:2 [ "identificador" => "sec0105" "titulo" => "Pentoxifylline" ] 1 => array:2 [ "identificador" => "sec0110" "titulo" => "Ascorbic Acid and Bioflavonoids (Rutin/Rutoside)" ] ] ] 3 => array:2 [ "identificador" => "sec0115" "titulo" => "Other Treatments" ] ] ] 11 => array:2 [ "identificador" => "sec0120" "titulo" => "Conclusions" ] 12 => array:2 [ "identificador" => "sec0125" "titulo" => "Conflicts of Interest" ] 13 => array:2 [ "identificador" => "xack460587" "titulo" => "Acknowledgments" ] 14 => array:1 [ "titulo" => "References" ] ] ] "pdfFichero" => "main.pdf" "tienePdf" => true "fechaRecibido" => "2018-10-21" "fechaAceptado" => "2019-02-24" "PalabrasClave" => array:2 [ "en" => array:1 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Keywords" "identificador" => "xpalclavsec1227991" "palabras" => array:4 [ 0 => "Purpuric pigmented dermatosis" 1 => "Review" 2 => "Clinical presentation" 3 => "Treatment" ] ] ] "es" => array:1 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Palabras clave" "identificador" => "xpalclavsec1227992" "palabras" => array:4 [ 0 => "Dermatosis purpúrico pigmentadas" 1 => "Revisión" 2 => "Presentación clínica" 3 => "Tratamiento" ] ] ] ] "tieneResumen" => true "resumen" => array:2 [ "en" => array:2 [ "titulo" => "Abstract" "resumen" => "<span id="abst0005" class="elsevierStyleSection elsevierViewall"><p id="spar0070" class="elsevierStyleSimplePara elsevierViewall">The pigmented purpuric dermatoses (PPDs) are a group of benign, chronic diseases. The variants described to date represent different clinical presentations of the same entity, all having similar histopathologic characteristics. We provide an overview of the most common PPDs and describe their clinical, dermatopathologic, and epiluminescence features. PPDs are both rare and benign, and this, together with an as yet poor understanding of the pathogenic mechanisms involved, means that no standardized treatments exist. We review the treatments described to date. However, because most of the descriptions are based on isolated cases or small series, there is insufficient evidence to support the use of any of these treatments as first-line therapy.</p></span>" ] "es" => array:2 [ "titulo" => "Resumen" "resumen" => "<span id="abst0010" class="elsevierStyleSection elsevierViewall"><p id="spar0075" class="elsevierStyleSimplePara elsevierViewall">Las dermatosis purpúrico pigmentadas (DPP) son un grupo de enfermedades benignas y de curso crónico. Las variantes descritas representan distintas formas clínicas de una misma entidad con unas características histopatológicas comunes para todas ellas. Exponemos a continuación un resumen de las variedades más frecuentes, sus características clínicas, dermatopatológicas y de epiluminiscencia. Al tratarse de una entidad clínica poco frecuente, benigna, y no conocerse claramente los mecanismos patogénicos de la misma, no existen tratamientos estandarizados. Se revisan los tratamientos publicados hasta el momento, la mayoría de ellos basados en casos aislados o pequeñas series de casos, sin poder establecer un nivel de evidencia suficiente como para ser recomendado ninguno de ellos como tratamiento de elección.</p></span>" ] ] "NotaPie" => array:1 [ 0 => array:2 [ "etiqueta" => "☆" "nota" => "<p class="elsevierStyleNotepara" id="npar0005">Please cite this article as: Martínez Pallás I, Conejero del Mazo R, Lezcano Biosca V. Dermatosis purpúricas pigmentadas. Revisión de la literatura científica. Actas Dermosifiliogr. 2020;111:196–204.</p>" ] ] "multimedia" => array:11 [ 0 => array:8 [ "identificador" => "fig0005" "etiqueta" => "Figure 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 1547 "Ancho" => 2167 "Tamanyo" => 195004 ] ] "detalles" => array:1 [ 0 => array:3 [ "identificador" => "at0005" "detalle" => "Figure " "rol" => "short" ] ] "descripcion" => array:1 [ "en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Etiologic and pathogenic mechanism. One of the most widely accepted hypotheses is that T cells are activated by an antigenic stimulus and bind to endothelial cells, fibroblasts, and keratinocytes through the expression of adhesion molecules. TNF-α indicates tumor necrosis factor α ; ICAM-1, intercellular adhesion molecule-1; LFA-1, lymphocyte function antigen-1.</p>" ] ] 1 => array:8 [ "identificador" => "fig0010" "etiqueta" => "Figure 2" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr2.jpeg" "Alto" => 1662 "Ancho" => 755 "Tamanyo" => 204387 ] ] "detalles" => array:1 [ 0 => array:3 [ "identificador" => "at0010" "detalle" => "Figure " "rol" => "short" ] ] "descripcion" => array:1 [ "en" => "<p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">Schamberg disease. A, Orange-red macules that tend to coalesce, forming large plaques. B, Peripheral cayenne pepper spots.</p>" ] ] 2 => array:8 [ "identificador" => "fig0015" "etiqueta" => "Figure 3" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr3.jpeg" "Alto" => 579 "Ancho" => 905 "Tamanyo" => 67351 ] ] "detalles" => array:1 [ 0 => array:3 [ "identificador" => "at0015" "detalle" => "Figure " "rol" => "short" ] ] "descripcion" => array:1 [ "en" => "<p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">Lichen aureus. Solitary plaque comprising small coalescing yellow-orange macules on the leg.</p>" ] ] 3 => array:8 [ "identificador" => "fig0020" "etiqueta" => "Figure 4" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr4.jpeg" "Alto" => 680 "Ancho" => 904 "Tamanyo" => 76759 ] ] "detalles" => array:1 [ 0 => array:3 [ "identificador" => "at0020" "detalle" => "Figure " "rol" => "short" ] ] "descripcion" => array:1 [ "en" => "<p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">Majocchi disease. Annular red-violaceous lesions on the leg.</p>" ] ] 4 => array:8 [ "identificador" => "fig0025" "etiqueta" => "Figure 5" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr5.jpeg" "Alto" => 1636 "Ancho" => 805 "Tamanyo" => 528650 ] ] "detalles" => array:1 [ 0 => array:3 [ "identificador" => "at0025" "detalle" => "Figure " "rol" => "short" ] ] "descripcion" => array:1 [ "en" => "<p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">Histopathological features of Schamberg disease. A, Infiltrate involving small vessels in the superficial dermis. B, Lymphocytic infiltrate, with luminal narrowing and extravasated red blood cells.</p>" ] ] 5 => array:8 [ "identificador" => "fig0030" "etiqueta" => "Figure 6" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr6.jpeg" "Alto" => 665 "Ancho" => 805 "Tamanyo" => 252604 ] ] "detalles" => array:1 [ 0 => array:3 [ "identificador" => "at0030" "detalle" => "Figure " "rol" => "short" ] ] "descripcion" => array:1 [ "en" => "<p id="spar0030" class="elsevierStyleSimplePara elsevierViewall">Histopathologic features of lichen aureus. Band-like infiltrate in the papillary dermis and superficial perivascular infiltrate.</p>" ] ] 6 => array:8 [ "identificador" => "fig0035" "etiqueta" => "Figure 7" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr7.jpeg" "Alto" => 605 "Ancho" => 805 "Tamanyo" => 51446 ] ] "detalles" => array:1 [ 0 => array:3 [ "identificador" => "at0035" "detalle" => "Figure " "rol" => "short" ] ] "descripcion" => array:1 [ "en" => "<p id="spar0035" class="elsevierStyleSimplePara elsevierViewall">Dermoscopic features of Schamberg disease. Coppery-red background and red globules.</p>" ] ] 7 => array:8 [ "identificador" => "fig0040" "etiqueta" => "Figure 8" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr8.jpeg" "Alto" => 605 "Ancho" => 805 "Tamanyo" => 76549 ] ] "detalles" => array:1 [ 0 => array:3 [ "identificador" => "at0040" "detalle" => "Figure " "rol" => "short" ] ] "descripcion" => array:1 [ "en" => "<p id="spar0040" class="elsevierStyleSimplePara elsevierViewall">Dermoscopic features of lichen aureus. Brownish-red background with gray dots and a pigmented pseudo-network.</p>" ] ] 8 => array:8 [ "identificador" => "tbl0005" "etiqueta" => "Table 1" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "detalles" => array:1 [ 0 => array:3 [ "identificador" => "at0045" "detalle" => "Table " "rol" => "short" ] ] "tabla" => array:2 [ "leyenda" => "<p id="spar0050" class="elsevierStyleSimplePara elsevierViewall">Source: Kaplan et al.<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">8</span></a></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=""><tbody title="tbody"><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Sedatives \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">Phenobarbital, chlordiazepoxide, meprobamate \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Vitamins \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">Thiamine (B<span class="elsevierStyleInf">1</span>) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Diuretics \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">Furosemide \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Cardiovascular drugs \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">Nitroglycerine, bezafibrate, hydralazine, dipyridamole, sildenafil \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Antibiotics \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">Ampicillin \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Analgesics \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">Nonsteroidal anti-inflammatory drugs, aspirin, acetaminophenol \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Stimulants \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">Pseudoephedrine \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Hormones \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">Medroxyprogesterone acetate \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Antidiabetic drugs \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">Glipizide \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Chemotherapy agents \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">Topical 5-fluorouracil \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Antivirals \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">Interferon α \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Retinoids \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">Isotretinoin \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab2284703.png" ] ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0045" class="elsevierStyleSimplePara elsevierViewall">Drugs Associated With the Pigmented Purpuric Dermatoses.</p>" ] ] 9 => array:8 [ "identificador" => "tbl0010" "etiqueta" => "Table 2" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "detalles" => array:1 [ 0 => array:3 [ "identificador" => "at0050" "detalle" => "Table " "rol" => "short" ] ] "tabla" => array:1 [ "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"><th 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" scope="col" style="border-bottom: 2px solid black">Variant \t\t\t\t\t\t\n \t\t\t\t\t\t</th><th 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" scope="col" style="border-bottom: 2px solid black">Clinical Presentation \t\t\t\t\t\t\n \t\t\t\t\t\t</th><th 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" scope="col" style="border-bottom: 2px solid black">Location \t\t\t\t\t\t\n \t\t\t\t\t\t</th><th 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" scope="col" style="border-bottom: 2px solid black">Histopathologic Findings \t\t\t\t\t\t\n \t\t\t\t\t\t</th></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Schamberg disease \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">Red-orange macules with peripheral spots resembling grains of cayenne pepper \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">Lower limbs and occasionally trunk, arms, thighs, and buttocks \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">Lymphocytic infiltrate involving the superficial small vessels, extravasated red blood cells, and hemosiderin-laden macrophages \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Eczematoid purpura of Doucas and Kapetanakis \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">Similar to manifestations of Schamberg disease but with scaling and intense itching \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">Lower limbs \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">Infiltrate with higher number of neutrophils and epidermal spongiosis \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Pigmented purpuric lichenoid dermatosis of Gougerot and Blum \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">Violaceous lichenoid papules that merge to form plaques \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">Lower limbs \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">Band-like dermal infiltrate \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Lichen aureus \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">Isolated persistent red-orange plaque and purpuric lesions \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">Lower limbs \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">Unchanged epidermis and band-like dermal infiltrate with Grenz area \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t">Majocchi disease \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">Peripherally extending plaques with telangiectatic punta at edges and fading in the central area \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">Lower limbs and trunk \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">Identical to Schamberg disease \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab2284701.png" ] ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0055" class="elsevierStyleSimplePara elsevierViewall">Clinical and Histopathologic Characteristics of the Pigmented Purpuric Dermatoses.</p>" ] ] 10 => array:8 [ "identificador" => "tbl0015" "etiqueta" => "Table 3" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "detalles" => array:1 [ 0 => array:3 [ "identificador" => "at0055" "detalle" => "Table " "rol" => "short" ] ] "tabla" => array:2 [ "leyenda" => "<p id="spar0065" class="elsevierStyleSimplePara elsevierViewall">Source: Sardana et al.<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a>, Kim et al.,<a class="elsevierStyleCrossRef" href="#bib0125"><span class="elsevierStyleSup">25</span></a> and Risikesan et al.<a class="elsevierStyleCrossRef" href="#bib0130"><span class="elsevierStyleSup">26</span></a></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"><th 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" scope="col" style="border-bottom: 2px solid black">Clinical Entities \t\t\t\t\t\t\n \t\t\t\t\t\t</th><th 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" scope="col" style="border-bottom: 2px solid black">Main characteristics \t\t\t\t\t\t\n \t\t\t\t\t\t</th></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Drug-hypersensitivity reactions</span> \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">Recent use of causative drug \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Carbamazepine, meprobamate, chlordiazepoxide, furosemide, nitroglycerine, vitamin B<span class="elsevierStyleInf">1</span>, and topical 5-fluorouracil \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"> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Purpuric contact dermatitis to clothing</span> \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">Lesions confined to areas of the skin in contact with clothing; intense itching \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleHsp" style=""></span>Wool, coloring agents \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"> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Venous stasis purpura</span> \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">Signs of chronic venous insufficiency: swelling, varicose veins, feeling of heaviness, venous ulcers \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \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">Hemosiderin deposition in deep dermis \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Purpura due to thrombocytopenia</span> \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">Associated with platelet count < 100–150000/μL \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Senile purpura</span> \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">In elderly patients, purpura can be associated with antiplatelet, anticoagulant, or corticosteroid use \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Purpuric exanthema due to viral infection</span> \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">Other signs of infection \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Leukocytoclastic vasculitis</span> \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">Palpable purpuric lesions \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \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">On histology: fibrinoid necrosis, endothelial swelling, and leukocytoclasis \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Schönlein-Henoch purpura</span> \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">Age, 3–15 years; symmetric purpura affecting legs and buttocks; joint and abdominal pain \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Kaposi sarcoma</span> \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">Affects elderly or immunosuppressed patients \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"> \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">On histology: spindle cells in the dermis forming irregular vascular lumina \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="\n \t\t\t\t\ttable-entry\n \t\t\t\t ; entry_with_role_rowhead " align="left" valign="\n \t\t\t\t\ttop\n \t\t\t\t"><span class="elsevierStyleItalic">Purpuric mycosis fungoides</span> \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">Onset > 1 year; disseminated, monoclonal profile in infiltrate and loss of CD7 \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab2284702.png" ] ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0060" class="elsevierStyleSimplePara elsevierViewall">Differential Diagnosis for the Pigmented Purpuric Dermatoses.</p>" ] ] ] "bibliografia" => array:2 [ "titulo" => "References" "seccion" => array:1 [ 0 => array:2 [ "identificador" => "bibs0005" "bibliografiaReferencia" => array:62 [ 0 => array:3 [ "identificador" => "bib0005" "etiqueta" => "1" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Purpura" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:1 [ 0 => "T.A. 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año/Mes | Html | Total | |
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2021 Diciembre | 403 | 82 | 485 |
2021 Noviembre | 439 | 81 | 520 |
2021 Octubre | 419 | 82 | 501 |
2021 Septiembre | 445 | 68 | 513 |
2021 Agosto | 429 | 96 | 525 |
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2020 Diciembre | 315 | 65 | 380 |
2020 Noviembre | 365 | 54 | 419 |
2020 Octubre | 180 | 40 | 220 |
2020 Septiembre | 299 | 36 | 335 |
2020 Agosto | 219 | 47 | 266 |
2020 Julio | 190 | 57 | 247 |
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2020 Mayo | 131 | 73 | 204 |
2020 Abril | 55 | 36 | 91 |
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