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Maturing papillomatous nevoid melanoma in the scalp mimicking recurrent melanocytic nevus: A case report of previously undescribed subtype of nevoid melanoma.
Tsujimura, Marina; Kaku, Yo; Takeuchi, Yasuhide; Ishida, Yoshihiro; Fujimoto, Masakazu; Usui, Shunya; Yamada, Yosuke; Ogawa, Seishi; Shea, Christopher R; Haga, Hironori.
  • Tsujimura M; Department of Diagnostic Pathology, Kyoto University Hospital, Kyoto, Japan.
  • Kaku Y; Department of Dermatology, Kyoto University Hospital, Kyoto, Japan.
  • Takeuchi Y; Department of Diagnostic Pathology, Kyoto University Hospital, Kyoto, Japan.
  • Ishida Y; Department of Dermatology, Kyoto University Hospital, Kyoto, Japan.
  • Fujimoto M; Department of Diagnostic Pathology, Kyoto University Hospital, Kyoto, Japan.
  • Usui S; Department of Dermatology, Kyoto University Hospital, Kyoto, Japan.
  • Yamada Y; Department of Diagnostic Pathology, Kyoto University Hospital, Kyoto, Japan.
  • Ogawa S; Department of Pathology and Tumor Biology, Kyoto University, Kyoto, Japan.
  • Shea CR; Department of Medicine, Section of Dermatology, The University of Chicago Medicine, Chicago, Illinois, USA.
  • Haga H; Department of Diagnostic Pathology, Kyoto University Hospital, Kyoto, Japan.
Pathol Int ; 72(1): 59-64, 2022 Jan.
Article en En | MEDLINE | ID: mdl-34637567
Nevoid melanoma is a subtype of melanoma that histologically resembles a melanocytic nevus. Two subtypes have been proposed for nevoid melanoma, namely papillomatous and maturing. Here, we report the case of a 67-year-old woman who developed two nevoid melanomas on her scalp with composite histological features of papillomatous and maturing subtypes after electrocautery of a nearby solitary scalp papule. The histology of both lesions was very similar, papillary in shape, and both comprised two melanocyte populations, including large atypical melanocytes and small non-atypical melanocytes. Whole-exome sequencing was performed in one of the two lesions, which revealed a high mutation burden (17 mutations/megabase) with co-deletion of CDKN2A. Additional immunohistochemistry revealed that the large and small melanocytes in both lesions were completely negative for p16 and MTAP. A final diagnosis of nevoid melanoma was made. To our knowledge, this is the first report of a nevoid melanoma with both features of papillomatous and maturing subtypes. Pathologists should be aware of this subtype of melanoma to avoid misdiagnosis as a mitotically active melanocytic nevus. In this case, immunohistochemistry for p16 and MTAP, in addition to molecular analysis, helped in the final diagnosis.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias Cutáneas / Diagnóstico Diferencial / Melanoma / Nevo Pigmentado Tipo de estudio: Diagnostic_studies Límite: Female / Humans / Middle aged Idioma: En Año: 2022 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias Cutáneas / Diagnóstico Diferencial / Melanoma / Nevo Pigmentado Tipo de estudio: Diagnostic_studies Límite: Female / Humans / Middle aged Idioma: En Año: 2022 Tipo del documento: Article