Practical Dermoscopy
BAP1-inactivated Melanocytic Tumor: Dermoscopic Features to Aid Diagnosis
Tumor melanocítico inactivado a BAP1: claves para su diagnóstico dermatoscópico
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Yélamos" "autores" => array:3 [ 0 => array:4 [ "nombre" => "X." "apellidos" => "Fustà-Novell" "email" => array:1 [ 0 => "xfusta@althaia.cat" ] "referencia" => array:2 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "aff0005" ] 1 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">*</span>" "identificador" => "cor0005" ] ] ] 1 => array:3 [ "nombre" => "A." "apellidos" => "García-Herrera" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">b</span>" "identificador" => "aff0010" ] ] ] 2 => array:3 [ "nombre" => "O." "apellidos" => "Yélamos" "referencia" => array:1 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">c</span>" "identificador" => "aff0015" ] ] ] ] "afiliaciones" => array:3 [ 0 => array:3 [ "entidad" => "Servicio de Dermatología, Althaia, Xarxa Assistencial Universitària de Manresa, Spain" "etiqueta" => "a" "identificador" => "aff0005" ] 1 => array:3 [ "entidad" => "Servicio de Anatomía Patológica, Hospital Clínic de Barcelona, Universitat de Barcelona, Spain" "etiqueta" => "b" "identificador" => "aff0010" ] 2 => array:3 [ "entidad" => "Servicio de Dermatología, Hospital de la Santa Creu i Sant Pau, Universitat Autònoma de Barcelona, Spain" "etiqueta" => "c" "identificador" => "aff0015" ] ] "correspondencia" => array:1 [ 0 => array:3 [ "identificador" => "cor0005" "etiqueta" => "⁎" "correspondencia" => "Corresponding author." ] ] ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Tumor melanocítico inactivado a BAP1: claves para su diagnóstico dermatoscópico" ] ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:7 [ "identificador" => "fig0015" "etiqueta" => "Figure 3" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr3.jpeg" "Alto" => 647 "Ancho" => 848 "Tamanyo" => 157252 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">Histologic images. A, Combined polypoid intradermal melanocytic proliferation with a peripheral melanocytic population consistent with a common nevus (arrow) and a second central spitzoid population (asterisks). Note the moderate lymphocytic inflammatory infiltrate (hematoxylin–eosin, original magnification 40). B, Common nevus at the periphery comprising nests of small clonal melanocytes (arrow). Central spitzoid population, with an abundant eosinophilic cytoplasm and discrete nuclear pleomorphism and no evidence of mitosis (hematoxylin–eosin, original magnification 100). C and D, Immunohistochemistry showing loss of BAP1 expression in the spitzoid (asterisks) but not common nevus component (arrow) of the lesion (BAP1, original magnification 100 and 200, respectively).</p>" ] ] ] "textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Case Report</span><p id="par0005" class="elsevierStylePara elsevierViewall">A 25-year-old man presented with a lesion in the right pectoral area that had grown progressively since its appearance 2 years earlier. He denied a personal or family history of skin cancer or other cancers. Physical examination revealed a firm orange papule with a diameter of 5<span class="elsevierStyleHsp" style=""></span>mm and perilesional erythema (<a class="elsevierStyleCrossRef" href="#fig0005">Fig. 1</a>). No similar lesions were observed elsewhere.</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0010" class="elsevierStylePara elsevierViewall">Dermoscopy showed a structureless, homogeneous orange pattern with multiple serpentine vessels distributed throughout the lesion and a branched, larger-caliber telangiectatic vessel crossing the lesion eccentrically (<a class="elsevierStyleCrossRef" href="#fig0010">Fig. 2</a>). Histologic and immunohistochemical findings are shown in <a class="elsevierStyleCrossRef" href="#fig0015">Fig. 3</a>.</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Diagnosis</span><p id="par0020" class="elsevierStylePara elsevierViewall">BAP1-inactivated melanocytic tumor (BIMT).</p></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Comment</span><p id="par0025" class="elsevierStylePara elsevierViewall">BIMTs, informally known as bapomas, are melanocytic tumors with a unique genetic profile in that they show inactivation of BRCA1 associated protein 1 (<span class="elsevierStyleItalic">BAP1</span>), a tumor suppressor gene.<a class="elsevierStyleCrossRefs" href="#bib0035"><span class="elsevierStyleSup">1,2</span></a> Some authors consider BIMTs to be a variant of Spitz nevus, while others consider them to be a separate entity with some overlapping clinical and cytological characteristics.<a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">2,3</span></a> Although BIMTs are not malignant (there have been no reports of malignant behavior or potential), multiple lesions are a marker of a familial autosomal dominant cancer syndrome caused by a germline inactivating <span class="elsevierStyleItalic">BAP1</span> mutation.<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">4</span></a> Diagnosis of BIMT is important, as the mutation predisposes to several cancers, including pleural and peritoneal mesothelioma, uveal and cutaneous melanoma, nonmelanoma skin cancer, meningioma, lung adenocarcinoma, and renal cell carcinoma.<a class="elsevierStyleCrossRefs" href="#bib0050"><span class="elsevierStyleSup">4,5</span></a> Some studies have suggested that BIMTs precede other cancers, with a mean age at diagnosis of 30 years.<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">6</span></a> Sporadic BIMTs (i.e., tumors without a syndromic association), have also been described.<a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">2,6</span></a> We did not conduct a germline genetic study, as there was no personal or family history of cancer, and we observed no similar or suspicious skin lesions. The patient was referred for annual clinical follow-up. At the time of writing, 2 years later, he has not developed any other lesions.</p><p id="par0030" class="elsevierStylePara elsevierViewall">Clinically, BIMTs are nonspecific, polymorphous lesions. They generally present as pink or orange papulonodular lesions. The differential diagnosis is broad and includes both melanocytic tumors (intradermal melanocytic nevus, Spitz nevus, melanoma) and nonmelanocytic tumors (neurofibroma, xanthogranuloma, basal cell carcinoma).<a class="elsevierStyleCrossRefs" href="#bib0035"><span class="elsevierStyleSup">1,2</span></a> The dermoscopic features of BIMTs were recently described<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">2</span></a> and can be very useful for aiding diagnosis. Several dermoscopic patterns have been identified: a structureless pink-orange pattern with linear peripheral vessels; a structureless, homogeneous, pink-orange pattern; a structureless pink-orange pattern with radial vessels; a structureless homogeneous pink-orange pattern with atypical eccentric globules; and a network pattern with raised, structureless pink-orange areas.<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">2</span></a> The last 2 patterns may be more common in patients with multiple BIMTs and a known germline mutation.<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">2</span></a> The globular pattern, by contrast, is uncommon in BIMTs, and appears to be a negative predictor of germline mutations in <span class="elsevierStyleItalic">BAP1</span>, as it has only been described in sporadic BIMTs.<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">2</span></a> Dermoscopy in the current case showed a variant of the structureless pink-orange pattern with linear vessels (one of the most common patterns described), with both central and peripheral vessels. The use of contact dermoscopy in the study of dermoscopic features of BIMTs by the International Dermoscopy Society<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">2</span></a> may explain why vessels were not seen in the center of the tumors.</p><p id="par0035" class="elsevierStylePara elsevierViewall">Histologically, BIMTs are similar to Spitz nevi, but they do not show epidermal hyperplasia, hypergranulosis, or Kamino bodies.<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">2</span></a> They typically show 2 cell populations: nevus cells with a conventional appearance located at the periphery of the lesion and atypical, epithelioid cells with a spitzoid appearance that lack melanin.<a class="elsevierStyleCrossRefs" href="#bib0035"><span class="elsevierStyleSup">1,6</span></a> Immunohistochemical staining shows clear nuclear loss of BAP1 in this atypical spitzoid population.<a class="elsevierStyleCrossRefs" href="#bib0035"><span class="elsevierStyleSup">1,6</span></a></p><p id="par0040" class="elsevierStylePara elsevierViewall">In conclusion, BIMTs require a high index of clinical suspicion, but their diagnosis may have important prognostic and follow-up implications. Familiarity with dermoscopic features can help.</p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Conflicts of Interest</span><p id="par0045" class="elsevierStylePara elsevierViewall">The authors declare that they have no conflicts of interest.</p></span></span>" "textoCompletoSecciones" => array:1 [ "secciones" => array:5 [ 0 => array:2 [ "identificador" => "sec0005" "titulo" => "Case Report" ] 1 => array:2 [ "identificador" => "sec0010" "titulo" => "Diagnosis" ] 2 => array:2 [ "identificador" => "sec0015" "titulo" => "Comment" ] 3 => array:2 [ "identificador" => "sec0020" "titulo" => "Conflicts of Interest" ] 4 => array:1 [ "titulo" => "References" ] ] ] "pdfFichero" => "main.pdf" "tienePdf" => true "multimedia" => array:3 [ 0 => array:7 [ "identificador" => "fig0005" "etiqueta" => "Figure 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 482 "Ancho" => 646 "Tamanyo" => 62402 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Orange papule with a diameter of 5<span class="elsevierStyleHsp" style=""></span>mm and perilesional erythema in the right pectoral area.</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" => 528 "Ancho" => 646 "Tamanyo" => 40106 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">Dermoscopic image showing a structureless, homogeneous orange pattern with multiple serpentine vessels distributed throughout the lesion and a branched, larger-caliber telangiectatic vessel crossing the lesion eccentrically.</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" => 647 "Ancho" => 848 "Tamanyo" => 157252 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">Histologic images. A, Combined polypoid intradermal melanocytic proliferation with a peripheral melanocytic population consistent with a common nevus (arrow) and a second central spitzoid population (asterisks). Note the moderate lymphocytic inflammatory infiltrate (hematoxylin–eosin, original magnification 40). B, Common nevus at the periphery comprising nests of small clonal melanocytes (arrow). Central spitzoid population, with an abundant eosinophilic cytoplasm and discrete nuclear pleomorphism and no evidence of mitosis (hematoxylin–eosin, original magnification 100). C and D, Immunohistochemistry showing loss of BAP1 expression in the spitzoid (asterisks) but not common nevus component (arrow) of the lesion (BAP1, original magnification 100 and 200, respectively).</p>" ] ] ] "bibliografia" => array:2 [ "titulo" => "References" "seccion" => array:1 [ 0 => array:2 [ "identificador" => "bibs0015" "bibliografiaReferencia" => array:6 [ 0 => array:3 [ "identificador" => "bib0035" "etiqueta" => "1" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Germline mutations in BAP1 predispose to melanocytic tumors" "autores" => array:1 [ 0 => array:2 [ "etal" => true "autores" => array:6 [ 0 => "T. Wiesner" 1 => "A.C. Obenauf" 2 => "R. Murali" 3 => "I. Fried" 4 => "K.G. Griewank" 5 => "P. 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| Year/Month | Html | Total | |
|---|---|---|---|
| 2024 November | 16 | 11 | 27 |
| 2024 October | 110 | 65 | 175 |
| 2024 September | 122 | 63 | 185 |
| 2024 August | 159 | 86 | 245 |
| 2024 July | 103 | 56 | 159 |
| 2024 June | 114 | 69 | 183 |
| 2024 May | 124 | 47 | 171 |
| 2024 April | 95 | 42 | 137 |
| 2024 March | 80 | 61 | 141 |
| 2024 February | 71 | 33 | 104 |
| 2024 January | 96 | 36 | 132 |
| 2023 December | 154 | 22 | 176 |
| 2023 November | 97 | 32 | 129 |
| 2023 October | 140 | 35 | 175 |
| 2023 September | 104 | 27 | 131 |
| 2023 August | 85 | 13 | 98 |
| 2023 July | 91 | 36 | 127 |
| 2023 June | 78 | 25 | 103 |
| 2023 May | 73 | 28 | 101 |
| 2023 April | 56 | 30 | 86 |
| 2023 March | 100 | 31 | 131 |
| 2023 February | 134 | 49 | 183 |
| 2023 January | 95 | 64 | 159 |
| 2022 December | 82 | 79 | 161 |
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