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Erupción liquenoide en un niño con características clínicas de PLEVA que histológicamente muestra atipia linfocitaria. (HE × 200.) B. Contiene abundantes células linfoides CD30+. (CD30 [inmunohistoquímica] × 200.)</p>" ] ] ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "M.T. Fernández-Figueras, L. Puig" "autores" => array:2 [ 0 => array:2 [ "nombre" => "M.T." "apellidos" => "Fernández-Figueras" ] 1 => array:2 [ "nombre" => "L." "apellidos" => "Puig" ] ] ] ] ] "idiomaDefecto" => "es" "Traduccion" => array:1 [ "en" => array:9 [ "pii" => "S1578219013000334" "doi" => "10.1016/j.adengl.2012.10.007" "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/S1578219013000334?idApp=UINPBA000044" ] ] "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S0001731012004802?idApp=UINPBA000044" "url" => "/00017310/0000010400000003/v1_201304241344/S0001731012004802/v1_201304241344/es/main.assets" ] ] "itemSiguiente" => array:19 [ "pii" => "S1578219013000346" "issn" => "15782190" "doi" => "10.1016/j.adengl.2011.12.011" "estado" => "S300" "fechaPublicacion" => "2013-04-01" "aid" => "635" "copyright" => "Elsevier España, S.L. and AEDV" "documento" => "article" "crossmark" => 0 "subdocumento" => "ssu" "cita" => "Actas Dermosifiliogr. 2013;104:212-9" "abierto" => array:3 [ "ES" => true "ES2" => true "LATM" => true ] "gratuito" => true "lecturas" => array:2 [ "total" => 6333 "formatos" => array:3 [ "EPUB" => 40 "HTML" => 5585 "PDF" => 708 ] ] "en" => array:13 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Novelties in Dermatology</span>" "titulo" => "New Developments in Erythropoietic Porphyrias" "tienePdf" => "en" "tieneTextoCompleto" => "en" "tieneResumen" => array:2 [ 0 => "en" 1 => "es" ] "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "212" "paginaFinal" => "219" ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Novedades en las porfirias eritropoyéticas" ] ] "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" => "fig0035" "etiqueta" => "Figure 7" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr7.jpeg" "Alto" => 738 "Ancho" => 1610 "Tamanyo" => 88004 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0045" class="elsevierStyleSimplePara elsevierViewall">A, Yellowish coloration of the teeth of a child with congenital erythropoietic porphyria. B, Red fluorescence (erythrodontia) can be readily observed under Wood light.</p>" ] ] ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "E. Darwich, C. Herrero" "autores" => array:2 [ 0 => array:2 [ "nombre" => "E." "apellidos" => "Darwich" ] 1 => array:2 [ "nombre" => "C." 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A, Low-power magnification. B, Detail of neoplastic cells with a granular cytoplasm. C, The same specimen studied immunohistochemically with calretinin. D, Detail of calretinin-positive neoplastic cells.</p>" ] ] ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "L. Fuertes, C. Santonja, H. Kutzner, L. Requena" "autores" => array:4 [ 0 => array:2 [ "nombre" => "L." "apellidos" => "Fuertes" ] 1 => array:2 [ "nombre" => "C." "apellidos" => "Santonja" ] 2 => array:2 [ "nombre" => "H." "apellidos" => "Kutzner" ] 3 => array:2 [ "nombre" => "L." 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Fernández-Figueras, L. Puig" "autores" => array:2 [ 0 => array:4 [ "nombre" => "M.T." "apellidos" => "Fernández-Figueras" "email" => array:1 [ 0 => "maiteffig@gmail.com" ] "referencia" => array:3 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "aff0005" ] 1 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">b</span>" "identificador" => "aff0010" ] 2 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">¿</span>" "identificador" => "cor0005" ] ] ] 1 => array:3 [ "nombre" => "L." "apellidos" => "Puig" "referencia" => array:2 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">b</span>" "identificador" => "aff0010" ] 1 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">c</span>" "identificador" => "aff0015" ] ] ] ] "afiliaciones" => array:3 [ 0 => array:3 [ "entidad" => "Servicio de Anatomía Patológica, Hospital Universitari Germans Trias i Pujol, Badalona, Spain" "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "aff0005" ] 1 => array:3 [ "entidad" => "Departamento de Ciencias Morfológicas, Universitat Autònoma de Barcelona, Barcelona, Spain" "etiqueta" => "<span class="elsevierStyleSup">b</span>" "identificador" => "aff0010" ] 2 => array:3 [ "entidad" => "Servicio de Dermatología, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain" "etiqueta" => "<span class="elsevierStyleSup">c</span>" "identificador" => "aff0015" ] ] "correspondencia" => array:1 [ 0 => array:3 [ "identificador" => "cor0005" "etiqueta" => "⁎" "correspondencia" => "Corresponding author." ] ] ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Actualización en dermatopatología" ] ] "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" => 2475 "Ancho" => 1665 "Tamanyo" => 883773 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">A, The presence of small intracapsular nodal nevi in the sentinel lymph nodes of a melanoma is not uncommon, and this phenomenon can cause diagnostic difficulties when the primary tumor is a nevoid melanoma. (Hematoxylin-eosin, original magnification x200.) B, The preservation of p16 expression could be an additional indication of a benign neoplasm. (p16, original magnification x200.).</p>" ] ] ] "textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Introduction</span><p id="par0005" class="elsevierStylePara elsevierViewall">The past year has seen a wealth of new developments in dermatopathology, many of which are related to technical progress and advances in treatment. This short review covers some of the developments that may have the greatest impact on the pathological diagnosis of dermatological disorders in the following 6 main areas: melanocytic proliferations, inflammatory diseases (including drug-induced reactions), lymphoproliferative disorders, adnexal diseases, epidermal tumors, and mesenchymal tumors.</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Melanocytic Proliferations</span><p id="par0010" class="elsevierStylePara elsevierViewall">Melanoma has been one of the prominent topics in dermatopathology in recent years. The recent introduction of fluorescent in situ hybridization as a ancillary diagnostic test in the identification of malignant melanocytic tumors was a major advance in an area that had languished for decades.<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> Unfortunately, the evidence shows that commercially available diagnostic kits providing a set of probes targeting chromosomes 6 and 11 are inadequate in problematic tumors.<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2–4</span></a> The sensitivity and specificity obtained in ambiguous tumors is lower than expected. To optimize the results obtained, new probes should be added to the diagnostic kit, possibly targeting gene regions on chromosome 9. However, it is increasingly clear that the genetic aberrations present in each melanoma correlate with the tumor's clinical and pathologic features and biological behavior,<a class="elsevierStyleCrossRefs" href="#bib0025"><span class="elsevierStyleSup">5,6</span></a> and that they can help to elucidate the considerable differences in the clinical course of melanomas that are apparently in the same stage.</p><p id="par0015" class="elsevierStylePara elsevierViewall">Today, from a practical standpoint, the most accessible and manageable techniques in most pathology laboratories are immunohistochemical studies. Thus, studies that demonstrate the usefulness of immunohistochemical markers are of particular interest. One such example is a study showing CD10 expression to be an independent predictor of poor prognosis in melanoma.<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">7</span></a> Several studies have shown an association between the loss of immunohistochemical p16 expression and malignant transformation in melanocytic lesions. This finding may be a useful aid in the differentiation between Spitz nevus and childhood melanoma,<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">8</span></a> and between nodal nevi in sentinel lymph nodes and small melanoma metastases (<a class="elsevierStyleCrossRef" href="#fig0005">Fig. 1</a>).<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">9</span></a> The usefulness of p16 as a marker is less clear in other lesions, such as pigmented spindle cell nevi.<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a> Furthermore, a loss of p16 expression is typically observed in patients with dysplastic nevi, in which its absence is an initial step in the development of melanoma.<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">10</span></a></p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0020" class="elsevierStylePara elsevierViewall">Two studies provided reassuring evidence concerning the low risk of metastases in Spitzoid lesions and atypical melanocytic proliferations in childhood.<a class="elsevierStyleCrossRefs" href="#bib0055"><span class="elsevierStyleSup">11,12</span></a> Angiotropism may explain why these lesions spread to sentinel lymph nodes but lack the potential to generate disseminated metastases: melanocytes may spread to the lymph nodes through the perivascular space, but lack the capacity to invade the lymphatic system or the bloodstream. The phenomenon, which is similar to perineural infiltration, is also observed in some melanomas (<a class="elsevierStyleCrossRef" href="#fig0010">Fig. 2</a>.) Cells that migrate to lymph nodes by means of this mechanism cannot strictly speaking be considered metastases. A group of highly regarded dermatopathologists advocate the use of the vascular markers D2-40 and CD34 to clearly define the relationship between tumor cells and vascular structures.<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">13</span></a></p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><p id="par0025" class="elsevierStylePara elsevierViewall">The introduction of ultrasound scanners into dermatology departments has opened the door to the possibility of using fine-needle aspiration biopsies to investigate superficial tumors and suspected metastatic lymph nodes (a practice that does not have to be restricted to interventional radiologists or pathologists; by analogy, some endocrinologists perform fine-needle aspiration biopsies of the thyroid). Some authors have proposed using fine-needle aspiration cytology to identify metastatic melanoma in sentinel nodes and suspicious lymph nodes.<a class="elsevierStyleCrossRefs" href="#bib0070"><span class="elsevierStyleSup">14,15</span></a> They report that a negative result on ultrasound study for a sentinel node is very reliable, and when metastasis is suspected, immediate cytologic diagnosis can be obtained using ultrasound-guided fine-needle aspiration biopsy. If the cytology is positive for metastasis, lymphadenectomy can be performed without further investigation, thus reducing morbidity and expenditure. Sonomorphologically suspicious nodes in which the presence of metastases is not detected by cytology should undergo complete study according to the usual protocols for sentinel nodes.</p><p id="par0030" class="elsevierStylePara elsevierViewall">Two new histopathologic variants of melanoma have been described this year. The first of these is a variant of superficial spreading melanoma characterized by large junctional melanocytic nests.<a class="elsevierStyleCrossRef" href="#bib0080"><span class="elsevierStyleSup">16</span></a> This variant may go undetected on histopathology study because it lacks many of the well-known microscopic diagnostic criteria of malignancy. It usually develops on areas of the skin with actinic damage and, although growth tends to be radial, it can infiltrate the dermis. The second, which is associated with inactivating germline mutations of <span class="elsevierStyleItalic">BAP1 (BRCA1 associated protein-1</span>),<a class="elsevierStyleCrossRef" href="#bib0085"><span class="elsevierStyleSup">0,17</span></a> is a new hereditary syndrome that predisposes patients to epithelioid melanocytic nevi, atypical Spitzoid proliferation, cutaneous and uveal melanoma, lung cancer, meningioma, mesothelioma, and other cancers.<a class="elsevierStyleCrossRef" href="#bib0090"><span class="elsevierStyleSup">18</span></a> Moreover, individuals who do not have this hereditary predisposition can also present atypical epithelioid melanocytic proliferations that harbor inactivating mutations of <span class="elsevierStyleItalic">BAP1</span> and concomitant <span class="elsevierStyleItalic">BRAF</span> mutations (<span class="elsevierStyleItalic">V-raf murine sarcoma viral oncogene homolog B1</span>).<a class="elsevierStyleCrossRef" href="#bib0095"><span class="elsevierStyleSup">19</span></a> Lesions associated with inactivation of <span class="elsevierStyleItalic">BAP1</span> are characterized by a lack of correlation between their microscopic appearance resembling an atypical Spitz nevi and a relatively unremarkable clinical appearance, similar to an Unna or Miescher nevus.</p><p id="par0035" class="elsevierStylePara elsevierViewall">Finally, the introduction of targeted treatment for metastatic melanomas that test positive for the <span class="elsevierStyleItalic">BRAF</span> mutation has led to the development of automated techniques for detecting this target; these new techniques are more sensitive than traditional polymerase chain reaction followed by sequencing. In line with the widespread and growing practice of creating alliances between the companies that market biomarker detection techniques and those that produce the drugs targeting those molecules, the company that markets a drug that inhibits the B-Raf protein also distributes the device that detects the mutation that determines its therapeutic indication. This device offers greater sensitivity and specificity than conventional sequencing techniques or polymerase chain reaction.</p></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Drug-Induced Reactions and Other Inflammatory Processes</span><p id="par0040" class="elsevierStylePara elsevierViewall">The introduction of new drugs often gives rise to the appearance of skin reactions with previously unknown histopathologic patterns, and the reactions to treatments targeting biomarkers are a good example of this phenomenon. In patients treated with vemurafenib—a B-Raf inhibitor indicated in melanomas with V600E mutations—various skin reactions have been described, including a lobular neutrophilic panniculitis<a class="elsevierStyleCrossRef" href="#bib0100"><span class="elsevierStyleSup">20</span></a> that is often painful and associated with arthritis; in such cases the microscopic changes are focal and sometimes very subtle. The lesions most often biopsied in patients receiving this treatment are wart-like proliferations with features that fall between common viral warts, keratoacanthomas, and squamous cell carcinomas (<a class="elsevierStyleCrossRef" href="#fig0015">Fig. 3</a>).<a class="elsevierStyleCrossRef" href="#bib0105"><span class="elsevierStyleSup">21</span></a> Patients receiving treatment with sorafenib,<a class="elsevierStyleCrossRef" href="#bib0110"><span class="elsevierStyleSup">22</span></a> which has been prescribed for metastatic melanoma harboring <span class="elsevierStyleItalic">KIT</span> mutations, among other indications, also develop epithelial proliferations that are not usually papillomatous but tend to form cysts and are frequently related to hair follicles. Sorafenib also produces manifestations similar to those of pityriasis rubra pilaris.<a class="elsevierStyleCrossRef" href="#bib0115"><span class="elsevierStyleSup">23</span></a></p><elsevierMultimedia ident="fig0015"></elsevierMultimedia><p id="par0045" class="elsevierStylePara elsevierViewall">Biologic therapies, first introduced some years ago, have also led to the emergence of several reactions that have now begun to be well characterized. A recent review of the adverse effects of tumor-necrosis-factor (TNF) antagonists included erythema multiforme-like and lupus erythematosus-like lesions in addition to the neutrophil-rich disorders (psoriasiform dermatitis, palmoplantar pustular psoriasis, pustular folliculitis, Sweet syndrome, neutrophilic eccrine hidradenitis, and leukocytoclastic vasculitis).<a class="elsevierStyleCrossRef" href="#bib0120"><span class="elsevierStyleSup">24</span></a> In another article, TNF antagonists were reported to have caused a pseudolymphomatous drug reaction.<a class="elsevierStyleCrossRef" href="#bib0125"><span class="elsevierStyleSup">25</span></a> Such reactions have also been reported in patients receiving ustekinumab.<a class="elsevierStyleCrossRef" href="#bib0130"><span class="elsevierStyleSup">26</span></a></p><p id="par0050" class="elsevierStylePara elsevierViewall">Continuing in the field of drug reactions, one recently published article refutes the idea that eosinophilia in subacute lupus erythematosus is an indicator of a drug reaction,<a class="elsevierStyleCrossRef" href="#bib0135"><span class="elsevierStyleSup">27</span></a> and another reviews a series of cases in which the initial clinical and pathological diagnosis of drug-induced reaction was subsequently proven to be inaccurate.<a class="elsevierStyleCrossRef" href="#bib0140"><span class="elsevierStyleSup">28</span></a> This last study suggests that the label of drug-induced reaction is overused in such cases, especially in the case of maculopapular eruptions.</p><p id="par0055" class="elsevierStylePara elsevierViewall">A recent study<a class="elsevierStyleCrossRef" href="#bib0145"><span class="elsevierStyleSup">29</span></a> called into question the prognostic value of the severity of inflammatory dermal infiltrate in toxic epidermal necrolysis.<a class="elsevierStyleCrossRef" href="#bib0150"><span class="elsevierStyleSup">30</span></a> The severity of dermal infiltrate had previously been considered to be directly correlated with the risk of death in the course of this disease. In that study, only the depth of the epidermal necrosis was shown to have prognostic significance, and even that was not an independent predictor.<a class="elsevierStyleCrossRef" href="#bib0145"><span class="elsevierStyleSup">29</span></a></p><p id="par0060" class="elsevierStylePara elsevierViewall">In severe leukocytoclastic vasculitis, exocytosis of neutrophils to the surface can lead to the appearance of microabscesses on the tips of papillae, mimicking dermatitis herpetiformis. The publication of a case of dermatitis herpetiformis that began with petechiae and leukocytoclastic vasculitis alerts us to the possibility of making the opposite mistake.<a class="elsevierStyleCrossRef" href="#bib0155"><span class="elsevierStyleSup">31</span></a> Four new cases of—mostly systemic—diffuse nonbullous neutrophilic lupus erythematosus were reported during the year, further defining a newly emerging entity that is very difficult to recognize microscopically.<a class="elsevierStyleCrossRef" href="#bib0160"><span class="elsevierStyleSup">32</span></a></p><p id="par0065" class="elsevierStylePara elsevierViewall">A rather curious study on biopsy samples destined for immunofluorescence testing examined the effect of accidental immersion of the samples in formalin before freezing.<a class="elsevierStyleCrossRef" href="#bib0165"><span class="elsevierStyleSup">33</span></a> Unsurprisingly, the study revealed that even 2<span class="elsevierStyleHsp" style=""></span>minutes of immersion in formalin led to complete loss of the staining characteristics in cases of pemphigus and under 10<span class="elsevierStyleHsp" style=""></span>minutes in those of pemphigoid. The most fascinating finding was that immunologic deposits in the dermatitis herpetiformis samples resisted up to 2<span class="elsevierStyleHsp" style=""></span>hours of immersion in formalin. It is also of note that, after prolonged immersion in formalin, keratinocyte nuclei acquire autofluorescence, thereby simulating lupus erythematosus.</p><p id="par0070" class="elsevierStylePara elsevierViewall">An international group of European dermatopathologists has collected and studied 13 cases of lesions that had the clinical appearance and behavior of acute pityriasis lichenoides, but in which the biopsy results included T-cell clonality and a large number of CD30<span class="elsevierStyleSup">+</span> cells, which often coexpressed CD8 (<a class="elsevierStyleCrossRef" href="#fig0020">Fig. 4</a>).<a class="elsevierStyleCrossRef" href="#bib0170"><span class="elsevierStyleSup">34</span></a> Not only do these lesions microscopically simulate lymphomatoid papulosis, they may, in fact, belong to the same spectrum as this disorder. The same authors also found evidence of parvovirus 19 DNA in 40% of the cases, a finding which, together with the immunophenotype consisting of CD8<span class="elsevierStyleSup">+</span> and CD30<span class="elsevierStyleSup">+</span> cells, suggests a possible viral etiology.<a class="elsevierStyleCrossRef" href="#bib0170"><span class="elsevierStyleSup">34</span></a></p><elsevierMultimedia ident="fig0020"></elsevierMultimedia><p id="par0075" class="elsevierStylePara elsevierViewall">Also described recently was a new pseudolymphomatous variant of granuloma annulare rich in CD8<span class="elsevierStyleSup">+</span> T cells, a new variant that has been added to the list of known forms of this disease (necrobiotic, incomplete or interstitial, and the rare sarcoid and tuberculoid forms).<a class="elsevierStyleCrossRef" href="#bib0175"><span class="elsevierStyleSup">35</span></a></p><p id="par0080" class="elsevierStylePara elsevierViewall">Also on the subject of pseudolymphomatous lesions, a case of lipoatrophic panniculitis with the microscopic appearance of panniculitis-like T-cell lymphoma was reported in a pediatric patient; the pathogenesis was probably autoimmune.<a class="elsevierStyleCrossRef" href="#bib0180"><span class="elsevierStyleSup">36</span></a> Other forms of panniculitis that may pose problems in the differential diagnostic are those caused by cutaneous and mucosal mucormycosis, which can convincingly mimic pancreatic or gouty panniculitis; this similarity may, in part, be explained by the ability of these fungi to produce extracellular lipase.<a class="elsevierStyleCrossRef" href="#bib0185"><span class="elsevierStyleSup">37</span></a></p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Lymphoproliferative Disorders</span><p id="par0085" class="elsevierStylePara elsevierViewall">The most interesting advance in the field of lymphomas has been the characterization of primary cutaneous CD4<span class="elsevierStyleSup">+</span> small-to-medium-sized pleomorphic T-cell lymphoma, a provisional entity in the World Health Organization (WHO) classification. Owing to the low aggressiveness of these tumors, especially in the case of single-lesion disease, they are considered to represent a clonal T-cell lymphoproliferative disorder with an indolent clinical course. This entity is characterized by a proliferation of follicular helper T cells characterized by the expression of PD-1 (programmed cell death 1), a feature that can be used to distinguish it from other types of cutaneous T-cell lymphomas.<a class="elsevierStyleCrossRef" href="#bib0190"><span class="elsevierStyleSup">38</span></a></p><p id="par0090" class="elsevierStylePara elsevierViewall">It is possible that the cases currently included in this provisional entity can be divided into 2 categories. Most of these patients present a low-grade lymphoproliferative disorder analogous to a pseudo-T-cell lymphoma (usually solitary lesions),<a class="elsevierStyleCrossRef" href="#bib0190"><span class="elsevierStyleSup">38</span></a> while a small number of them present a follicular helper T-cell lymphoma (usually multiple lesions), which has a much more aggressive biological behavior and requires intense treatment.<a class="elsevierStyleCrossRef" href="#bib0195"><span class="elsevierStyleSup">39</span></a> In these lymphomas, the presence of numerous B lymphocytes in the infiltrate and the expression of CD10 in the neoplastic lymphocytes may give rise to confusion with follicular lymphoma.</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Adnexal Diseases</span><p id="par0095" class="elsevierStylePara elsevierViewall">Two cases have recently been described of eruptive hyperplasia of ectopic sebaceous glands after episodes of epidermal erosion caused by scald in one case<a class="elsevierStyleCrossRef" href="#bib0200"><span class="elsevierStyleSup">40</span></a> and following Stevens-Johnson syndrome in the other.<a class="elsevierStyleCrossRef" href="#bib0205"><span class="elsevierStyleSup">41</span></a></p><p id="par0100" class="elsevierStylePara elsevierViewall">In the field of alopecia, 2 new diagnostic clues have been reported.<a class="elsevierStyleCrossRefs" href="#bib0210"><span class="elsevierStyleSup">42,43</span></a> The first report highlights the utility of polarized light microscopy to distinguish between the scars of scarring alopecia (which are polarizable) and the fibrous streamers of androgenic alopecia which, despite having a very similar microscopic appearance, do not polarize.<a class="elsevierStyleCrossRef" href="#bib0210"><span class="elsevierStyleSup">42</span></a> The second article, by the same authors, provides a clue to the diagnosis of frontal fibrosing alopecia, which the authors have called the follicular triad.<a class="elsevierStyleCrossRef" href="#bib0215"><span class="elsevierStyleSup">43</span></a> The term refers to the simultaneous involvement of follicles of 3 types (terminal, vellus, and intermediate) in all 3 stages of cycling (anagen, catagen, and telogen).<a class="elsevierStyleCrossRef" href="#bib0215"><span class="elsevierStyleSup">43</span></a> This sign can be very useful in identifying this variant of lichenoid alopecia, which is not restricted to the frontal region, but can affect the entire scalp and other areas of the skin. Another symptom that has recently been added is facial papules secondary to the involvement of facial vellus hair.<a class="elsevierStyleCrossRef" href="#bib0220"><span class="elsevierStyleSup">44</span></a></p><p id="par0105" class="elsevierStylePara elsevierViewall">Still on the subject of alopecia, 2 independent studies show that permanent alopecia caused by systemic chemotherapy has histologic features identical to those of androgenic alopecia, leading to diagnostic difficulties.<a class="elsevierStyleCrossRefs" href="#bib0225"><span class="elsevierStyleSup">45,46</span></a> Finally, a new way has been proposed to optimize the yield of a single punch biopsy using a technique that produces both horizontal sections, which are very useful in the diagnosis of alopecia, and vertical sections, which allow us to assess the involvement of the epidermis and the uppermost layer of the dermis, also a source of relevant information.<a class="elsevierStyleCrossRef" href="#bib0235"><span class="elsevierStyleSup">47</span></a> The technique involves transecting the biopsy approximately 1<span class="elsevierStyleHsp" style=""></span>mm below the skin surface and using this to obtain vertical sections (perpendicular to the epidermis) and then sectioning the lower portion to obtain horizontal sections (parallel to the epidermis).</p><p id="par0110" class="elsevierStylePara elsevierViewall">Moving on to the subject of adnexal tumors, one of the most striking items that appeared in the last year was the description of desmoplastic trichoepithelioma with perineural involvement, an extremely unusual feature in benign tumors but one that can no longer be considered a reliable sign of malignancy in this context.<a class="elsevierStyleCrossRef" href="#bib0240"><span class="elsevierStyleSup">48</span></a> Eosinophilia has also been proposed as a clue to the diagnosis of microcystic adnexal carcinoma.<a class="elsevierStyleCrossRef" href="#bib0245"><span class="elsevierStyleSup">49</span></a></p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Epidermal Tumors</span><p id="par0115" class="elsevierStylePara elsevierViewall">The introduction of hedgehog pathway inhibitors for the treatment of advanced basal cell carcinoma<a class="elsevierStyleCrossRef" href="#bib0250"><span class="elsevierStyleSup">50</span></a> has stimulated the publication of numerous reports on cases of aggressive basal cell carcinoma.<a class="elsevierStyleCrossRefs" href="#bib0255"><span class="elsevierStyleSup">51,52</span></a> It is unclear why some of these tumors have such a high malignant potential that they grow to a large size, invade deep tissues, and even produce metastases. In 1 review of the literature,<a class="elsevierStyleCrossRef" href="#bib0255"><span class="elsevierStyleSup">51</span></a> basosquamous cell carcinoma is cited as one of the most aggressive variants of this type of tumor and the one that most often metastasizes; however in another study the same variant, which is considered rare, is said to have a similar prognosis to typical basal cell carcinoma even in transplant recipients.<a class="elsevierStyleCrossRef" href="#bib0265"><span class="elsevierStyleSup">53</span></a> In any case, the authors of the latter advocate the use of the Ber-EP4 antibody (Clone Ber-EP4) to confirm the diagnosis of this tumor; this marker is positive in areas of basal cells and negative in those of squamous cells.<a class="elsevierStyleCrossRef" href="#bib0265"><span class="elsevierStyleSup">53</span></a> A group of Spanish authors have also made an interesting discovery with respect to Ber-EP4, observing that it stained both sides of the retraction spaces surrounding epithelial nests in basal cell carcinoma.<a class="elsevierStyleCrossRef" href="#bib0270"><span class="elsevierStyleSup">54</span></a> Ber-EP4, also known as EpCAM (epithelial cell adhesion molecule), is directed against a specific epithelial antigen (a surface glycoprotein), so that staining on the exterior aspect of the retraction spaces would appear to indicate that these are epithelial in nature. In short, the retraction spaces typical of basal cell carcinoma are not, as has always been thought, located between the epithelium and the stroma, but rather occupy a more peripheral portion of the epithelium.<a class="elsevierStyleCrossRef" href="#bib0270"><span class="elsevierStyleSup">54</span></a></p><p id="par0120" class="elsevierStylePara elsevierViewall">Finally, several articles have appeared confirming the predictive value of the new American Joint Committee on Cancer staging system for squamous cell carcinoma,<a class="elsevierStyleCrossRef" href="#bib0275"><span class="elsevierStyleSup">55</span></a> which includes indicators of poor prognosis not included in the TNM cancer staging system, such as poor histologic differentiation, thickness greater than 2<span class="elsevierStyleHsp" style=""></span>mm, a Clark level of IV or more, the presence of vascular and/or perineural invasion, and location on the ear or lip.</p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Mesenchymal Tumors</span><p id="par0125" class="elsevierStylePara elsevierViewall">A recent article confirmed that the expression of p63 is rare in mesenchymal tumors, and when it occurs is usually focal or weak, confirming the usefulness of this protein in identifying pseudosarcomatous carcinomas (<a class="elsevierStyleCrossRef" href="#fig0025">Fig. 5</a>).<a class="elsevierStyleCrossRef" href="#bib0280"><span class="elsevierStyleSup">56</span></a> Similarly, new studies have confirmed that the amplification of MYC (avian myelocytomatosis virus) is an excellent marker for the cutaneous angiosarcomas that appear after radiotherapy or in areas of lymphedema, distinguishing them from other postradiation malignancies and angiosarcomas unrelated to radiotherapy. Moreover, immunohistochemical overexpression is as reliable as fluorescent in situ hybridization for the detection of this marker.<a class="elsevierStyleCrossRefs" href="#bib0285"><span class="elsevierStyleSup">57,58</span></a></p><elsevierMultimedia ident="fig0025"></elsevierMultimedia><p id="par0130" class="elsevierStylePara elsevierViewall">Finally, the term pleomorphic dermal sarcoma has been proposed to denominate lesions that resemble atypical fibroxanthomas microscopically but produce deep tissue invasion, extensive necrosis, and/or lymphovascular or perineural invasion.<a class="elsevierStyleCrossRef" href="#bib0295"><span class="elsevierStyleSup">59</span></a> We have even had room for controversy in this area, such as that arising from the description of pseudomyogenic hemangioendothelioma, previously called epithelioid sarcoma-like hemangioendothelioma.<a class="elsevierStyleCrossRef" href="#bib0300"><span class="elsevierStyleSup">60</span></a></p></span><span id="sec0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Conclusion</span><p id="par0135" class="elsevierStylePara elsevierViewall">In conclusion, in a year full of new developments, significant advances have been made in the diagnosis, staging, and treatment of melanocytic lesions. New drug-induced reactions have been described, especially reactions to the drugs more recently introduced into the therapeutic arsenal. Important advances have been made in the characterization of primary cutaneous CD4<span class="elsevierStyleSup">+</span> small-to-medium-sized pleomorphic T-cell lymphoma, a provisional WHO entity that, in many cases, is consistent with T pseudolymphomas. Likewise, we have seen the publication of new diagnostic features for alopecia and reports on the presence of perineural invasion in desmoplastic trichoblastoma. In addition, there has been confirmation of the usefulness of p63 and MYC in the identification of pseudosarcomatous epithelial proliferations and angiosarcomas secondary to radiotherapy or arising on lymphedema. Likewise, it has been confirmed that there is an excellent correlation between the new American Joint Committee on Cancer staging system for squamous cell carcinoma of skin and the biological behavior of these lesions.</p><p id="par0140" class="elsevierStylePara elsevierViewall">These and other excellent advances which, for reasons of space, could not be included in this brief review, are a reflection of the brilliant scientific production that continuously enriches the field of dermatopathology and allows us to be very optimistic about the future of this discipline.</p></span><span id="sec0045" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Ethical Disclosures</span><span id="sec0050" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Protection of Human and Animal Subjects</span><p id="par0145" class="elsevierStylePara elsevierViewall">The authors state that no experiments were performed on humans or animals for this investigation.</p></span><span id="sec0055" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Confidentiality of Data</span><p id="par0150" class="elsevierStylePara elsevierViewall">The authors declare that they have followed the protocols of their workplace concerning the publication of patient data, and that all the patients included in this study have been appropriately informed and gave their written informed consent to participate in this study.</p></span><span id="sec0060" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Right to Privacy and Informed Consent</span><p id="par0155" class="elsevierStylePara elsevierViewall">The authors declare that no patient data appear in this article.</p></span></span><span id="sec0065" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle">Conflicts of Interest</span><p id="par0160" class="elsevierStylePara elsevierViewall">The authors declare that they have no conflicts of interest.</p></span></span>" "textoCompletoSecciones" => array:1 [ "secciones" => array:15 [ 0 => array:2 [ "identificador" => "xres97876" "titulo" => "Abstract" ] 1 => array:2 [ "identificador" => "xpalclavsec85032" "titulo" => "Keywords" ] 2 => array:2 [ "identificador" => "xres97877" "titulo" => "Resumen" ] 3 => array:2 [ "identificador" => "xpalclavsec85033" "titulo" => "Palabras clave" ] 4 => array:2 [ "identificador" => "sec0005" "titulo" => "Introduction" ] 5 => array:2 [ "identificador" => "sec0010" "titulo" => "Melanocytic Proliferations" ] 6 => array:2 [ "identificador" => "sec0015" "titulo" => "Drug-Induced Reactions and Other Inflammatory Processes" ] 7 => array:2 [ "identificador" => "sec0020" "titulo" => "Lymphoproliferative Disorders" ] 8 => array:2 [ "identificador" => "sec0025" "titulo" => "Adnexal Diseases" ] 9 => array:2 [ "identificador" => "sec0030" "titulo" => "Epidermal Tumors" ] 10 => array:2 [ "identificador" => "sec0035" "titulo" => "Mesenchymal Tumors" ] 11 => array:2 [ "identificador" => "sec0040" "titulo" => "Conclusion" ] 12 => array:3 [ "identificador" => "sec0045" "titulo" => "Ethical Disclosures" "secciones" => array:3 [ 0 => array:2 [ "identificador" => "sec0050" "titulo" => "Protection of Human and Animal Subjects" ] 1 => array:2 [ "identificador" => "sec0055" "titulo" => "Confidentiality of Data" ] 2 => array:2 [ "identificador" => "sec0060" "titulo" => "Right to Privacy and Informed Consent" ] ] ] 13 => array:2 [ "identificador" => "sec0065" "titulo" => "Conflicts of Interest" ] 14 => array:1 [ "titulo" => "References" ] ] ] "pdfFichero" => "main.pdf" "tienePdf" => true "fechaRecibido" => "2012-06-20" "fechaAceptado" => "2012-10-16" "PalabrasClave" => array:2 [ "en" => array:1 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Keywords" "identificador" => "xpalclavsec85032" "palabras" => array:3 [ 0 => "Update" 1 => "Dermatopathology" 2 => "Review" ] ] ] "es" => array:1 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Palabras clave" "identificador" => "xpalclavsec85033" "palabras" => array:3 [ 0 => "Actualización" 1 => "Dermatopatología" 2 => "Revisión" ] ] ] ] "tieneResumen" => true "resumen" => array:2 [ "en" => array:2 [ "titulo" => "Abstract" "resumen" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">This past year has seen a wealth of new developments in dermatopathology that appear to herald the dawning of a new era. Advances in molecular biology and the simplification of techniques have put molecular tests within reach of routine clinical practice and led to a radical change in our approach to lesions such as melanoma; in the future, the genetic characterization of these lesions will be an essential requirement for establishing diagnosis, prognosis, and therapy. Technological innovations have also reached dermatology departments: the introduction of ultrasound scans has propitiated the use of fine-needle aspiration cytology, which allows samples to be stained and studied immediately, thereby facilitating diagnosis of superficial and lymph-node lesions, and allowing staging of tumors such as melanoma. Targeted cancer therapies have led to the introduction of more sensitive and specific systems for identifying new targets, have reawakened interest in forgotten diseases such as aggressive basal cell carcinoma, and have led to dermatological reactions that, together with those caused by biologic drugs, we are just beginning to recognize. Consolidated techniques such as immunohistochemistry continue to advance with the addition of new antibodies that contribute considerably to improved diagnosis. New clinicopathologic diseases have also been described or characterized this year, including 2 new types of melanoma, and progress has been made in our knowledge of other diseases, such as primary cutaneous CD4<span class="elsevierStyleSup">+</span> small/medium-sized pleomorphic T-cell lymphoma. These topics, together with new developments in adnexal tumors, alopecia, and other lesions, will be discussed in this review.</p>" ] "es" => array:2 [ "titulo" => "Resumen" "resumen" => "<p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">Este último año ha sido rico en novedades dermatopatológicas que se vislumbran como el inicio de una nueva era. Los avances en las técnicas de biología molecular y su simplificación, que las hace asequibles al uso rutinario, han supuesto un cambio radical en el concepto de lesiones como el melanoma, cuya caracterización genética será en el futuro un requisito indispensable para establecer el diagnóstico, el pronóstico y la terapéutica. Las innovaciones tecnológicas también han llegado a los servicios de Dermatología; la introducción de ecógrafos ha propiciado el uso de técnicas de citología por punción-aspiración que pueden ser teñidas y estudiadas de manera inmediata, facilitando el diagnóstico de lesiones superficiales y ganglionares, y permitiendo la estadificación de neoplasias como el melanoma. La aparición de tratamientos oncológicos dirigidos contra «dianas terapéuticas» ha conllevado la introducción de sistemas más sensibles y específicos para su idetificación, ha reactivado el interés por patologías olvidadas como el carcinoma basocelular agresivo y ha comportado la aparición de reacciones dermatológicas que, junto con las secundarias a fármacos biológicos, empezamos a reconocer. Técnicas consolidadas como la inmunohistoquímica continúan progresando con la incorporación de nuevos anticuerpos que contribuyen de manera notable al diagnóstico. Este año, además, se han descrito o caracterizado nuevas entidades clinicopatológicas, y entre ellas 2 nuevos tipos de melanoma. También se ha avanzado en el conocimiento de otras, como el linfoma T pleomórfico CD4+ de células pequeñas/medianas. Estos temas, junto con novedades en tumores anexiales, alopecias y otras lesiones, serán comentados en esta revisión.</p>" ] ] "NotaPie" => array:1 [ 0 => array:2 [ "etiqueta" => "☆" "nota" => "<p class="elsevierStyleNotepara">Please cite this article as: Fernández-Figueras MT, Puig L. Actualización en dermatopatología. Actas Dermosifiliogr. 2013;104:204–11.</p>" ] ] "multimedia" => array:5 [ 0 => array:7 [ "identificador" => "fig0005" "etiqueta" => "Figure 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 2475 "Ancho" => 1665 "Tamanyo" => 883773 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">A, The presence of small intracapsular nodal nevi in the sentinel lymph nodes of a melanoma is not uncommon, and this phenomenon can cause diagnostic difficulties when the primary tumor is a nevoid melanoma. (Hematoxylin-eosin, original magnification x200.) B, The preservation of p16 expression could be an additional indication of a benign neoplasm. (p16, original magnification x200.).</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" => 1253 "Ancho" => 1665 "Tamanyo" => 380200 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">Melanoma demonstrating angiotropism and neurotropism. Angiotropism, a phenomenon analogous to neurotropism, is found in both benign and malignant melanocytic tumors. It could explain how melanocytes spread to lymph nodes without being true metastases. (Hematoxylin-eosin, original magnification x200.).</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" => 1253 "Ancho" => 1665 "Tamanyo" => 390872 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">Patient with metastatic melanoma treated with the B-Raf inhibitor vemurafenib: a papillomatous lesion showing scant atypia and columns of parakeratosis sometimes containing small amounts of hemorrhage, similar to common viral warts. (Hematoxylin-eosin, original magnification x400.).</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" => 2560 "Ancho" => 1665 "Tamanyo" => 1033341 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0030" class="elsevierStyleSimplePara elsevierViewall">A, Lichenoid eruption in a child. The lesion has the clinical features of pityriasis lichenoides et varioliformis acuta but demonstrates lymphocytic atypia. (Hematoxylin-eosin, original magnification x200.) B, The lesion contains abundant CD30<span class="elsevierStyleSup">+</span> lymphoid cells. (CD30, original magnification x200.).</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" => 2558 "Ancho" => 1665 "Tamanyo" => 793015 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0035" class="elsevierStyleSimplePara elsevierViewall">A, Dermis replaced by dense collagen surrounding spindle cells with a mesenchymal appearance. (Hematoxylin-eosin, original magnification x100.) B, p63 positivity demonstrates the epithelial origin and facilitates the diagnosis of spindle cell squamous cell carcinoma. (p63, original magnification x100.).</p>" ] ] ] "bibliografia" => array:2 [ "titulo" => "References" "seccion" => array:1 [ 0 => array:2 [ "identificador" => "bibs0005" "bibliografiaReferencia" => array:60 [ 0 => array:3 [ "identificador" => "bib0005" "etiqueta" => "1" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Fluorescence in situ hybridization (FISH) as an ancillary diagnostic tool in the diagnosis of melanoma" "autores" => array:1 [ 0 => array:2 [ "etal" => true "autores" => array:6 [ 0 => "P. Gerami" 1 => "S.S. Jewell" 2 => "L.E. Morrison" 3 => "B. Blondin" 4 => "J. Schulz" 5 => "T. 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Year/Month | Html | Total | |
---|---|---|---|
2024 November | 14 | 12 | 26 |
2024 October | 88 | 41 | 129 |
2024 September | 74 | 30 | 104 |
2024 August | 92 | 67 | 159 |
2024 July | 65 | 29 | 94 |
2024 June | 85 | 28 | 113 |
2024 May | 71 | 44 | 115 |
2024 April | 76 | 34 | 110 |
2024 March | 72 | 42 | 114 |
2024 February | 202 | 42 | 244 |
2024 January | 67 | 53 | 120 |
2023 December | 66 | 14 | 80 |
2023 November | 103 | 32 | 135 |
2023 October | 83 | 37 | 120 |
2023 September | 89 | 24 | 113 |
2023 August | 49 | 24 | 73 |
2023 July | 60 | 28 | 88 |
2023 June | 56 | 25 | 81 |
2023 May | 51 | 22 | 73 |
2023 April | 33 | 20 | 53 |
2023 March | 64 | 18 | 82 |
2023 February | 83 | 31 | 114 |
2023 January | 67 | 29 | 96 |
2022 December | 50 | 45 | 95 |
2022 November | 41 | 25 | 66 |
2022 October | 26 | 23 | 49 |
2022 September | 33 | 41 | 74 |
2022 August | 30 | 40 | 70 |
2022 July | 23 | 33 | 56 |
2022 June | 17 | 21 | 38 |
2022 May | 31 | 42 | 73 |
2022 April | 42 | 24 | 66 |
2022 March | 27 | 56 | 83 |
2022 February | 23 | 34 | 57 |
2022 January | 24 | 34 | 58 |
2021 December | 30 | 37 | 67 |
2021 November | 34 | 37 | 71 |
2021 October | 37 | 58 | 95 |
2021 September | 29 | 39 | 68 |
2021 August | 29 | 45 | 74 |
2021 July | 25 | 39 | 64 |
2021 June | 24 | 38 | 62 |
2021 May | 26 | 39 | 65 |
2021 April | 78 | 66 | 144 |
2021 March | 41 | 29 | 70 |
2021 February | 53 | 36 | 89 |
2021 January | 30 | 17 | 47 |
2020 December | 25 | 21 | 46 |
2020 November | 20 | 22 | 42 |
2020 October | 38 | 14 | 52 |
2020 September | 26 | 9 | 35 |
2020 August | 28 | 23 | 51 |
2020 July | 25 | 18 | 43 |
2020 June | 46 | 27 | 73 |
2020 May | 28 | 14 | 42 |
2020 April | 27 | 25 | 52 |
2020 March | 30 | 9 | 39 |
2020 February | 3 | 1 | 4 |
2020 January | 0 | 5 | 5 |
2019 December | 4 | 7 | 11 |
2019 November | 0 | 2 | 2 |
2019 September | 4 | 4 | 8 |
2019 August | 2 | 0 | 2 |
2019 July | 0 | 7 | 7 |
2019 June | 0 | 5 | 5 |
2019 May | 2 | 16 | 18 |
2019 April | 0 | 13 | 13 |
2019 March | 0 | 9 | 9 |
2019 February | 2 | 0 | 2 |
2019 January | 0 | 1 | 1 |
2018 December | 1 | 0 | 1 |
2018 November | 2 | 0 | 2 |
2018 September | 4 | 0 | 4 |
2018 March | 0 | 2 | 2 |
2018 February | 40 | 6 | 46 |
2018 January | 37 | 8 | 45 |
2017 December | 52 | 5 | 57 |
2017 November | 31 | 8 | 39 |
2017 October | 41 | 8 | 49 |
2017 September | 36 | 3 | 39 |
2017 August | 74 | 14 | 88 |
2017 July | 54 | 8 | 62 |
2017 June | 80 | 17 | 97 |
2017 May | 57 | 10 | 67 |
2017 April | 52 | 11 | 63 |
2017 March | 43 | 20 | 63 |
2017 February | 33 | 10 | 43 |
2017 January | 38 | 14 | 52 |
2016 December | 51 | 10 | 61 |
2016 November | 61 | 8 | 69 |
2016 October | 76 | 6 | 82 |
2016 September | 64 | 16 | 80 |
2016 August | 61 | 14 | 75 |
2016 July | 52 | 13 | 65 |
2016 June | 12 | 8 | 20 |
2016 May | 5 | 16 | 21 |
2016 April | 5 | 2 | 7 |
2016 March | 4 | 3 | 7 |
2016 February | 4 | 3 | 7 |
2016 January | 8 | 1 | 9 |
2015 December | 8 | 7 | 15 |
2015 November | 9 | 2 | 11 |
2015 October | 7 | 1 | 8 |
2015 September | 6 | 1 | 7 |
2015 August | 9 | 2 | 11 |
2015 July | 90 | 120 | 210 |
2015 June | 88 | 20 | 108 |
2015 May | 103 | 23 | 126 |
2015 April | 83 | 15 | 98 |
2015 March | 28 | 8 | 36 |
2015 February | 29 | 5 | 34 |
2015 January | 28 | 5 | 33 |
2014 December | 38 | 4 | 42 |
2014 November | 30 | 3 | 33 |
2014 October | 58 | 9 | 67 |
2014 September | 39 | 5 | 44 |
2014 August | 42 | 3 | 45 |
2014 July | 33 | 8 | 41 |
2014 June | 44 | 4 | 48 |
2014 May | 50 | 11 | 61 |
2014 April | 50 | 4 | 54 |
2014 March | 48 | 14 | 62 |
2014 February | 46 | 11 | 57 |
2014 January | 35 | 6 | 41 |
2013 December | 39 | 15 | 54 |
2013 November | 33 | 10 | 43 |
2013 October | 26 | 9 | 35 |
2013 September | 35 | 9 | 44 |
2013 August | 31 | 21 | 52 |
2013 July | 6 | 1 | 7 |
2013 June | 5 | 8 | 13 |
2013 May | 3 | 4 | 7 |
2013 April | 7 | 16 | 23 |