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Subungual melanoma with cartilaginous differentiation: Molecular insights.
Shaikh, Umayr; Shah, Payal; Jones, Victoria; Ramos-Rodriguez, Alvaro J; Sriharan, Aravindhan; Loo, Eric; Khan, Wahab A; Simmons, Brian; Cloutier, Jeffrey M.
Afiliación
  • Shaikh U; School of Medicine, Georgetown University, Washington, DC, USA.
  • Shah P; Department of Dermatology, Dartmouth Health, Lebanon, New Hampshire, USA.
  • Jones V; Department of Pathology and Laboratory Medicine, One Medical Center Drive, Dartmouth Health, Dartmouth Hitchcock Medical Center, Lebanon, New Hampshire, USA.
  • Ramos-Rodriguez AJ; Department of Pathology and Laboratory Medicine, One Medical Center Drive, Dartmouth Health, Dartmouth Hitchcock Medical Center, Lebanon, New Hampshire, USA.
  • Sriharan A; Department of Pathology and Laboratory Medicine, One Medical Center Drive, Dartmouth Health, Dartmouth Hitchcock Medical Center, Lebanon, New Hampshire, USA.
  • Loo E; Department of Pathology and Laboratory Medicine, One Medical Center Drive, Dartmouth Health, Dartmouth Hitchcock Medical Center, Lebanon, New Hampshire, USA.
  • Khan WA; Department of Pathology and Laboratory Medicine, One Medical Center Drive, Dartmouth Health, Dartmouth Hitchcock Medical Center, Lebanon, New Hampshire, USA.
  • Simmons B; Department of Dermatology, Dartmouth Health, Lebanon, New Hampshire, USA.
  • Cloutier JM; Department of Pathology and Laboratory Medicine, One Medical Center Drive, Dartmouth Health, Dartmouth Hitchcock Medical Center, Lebanon, New Hampshire, USA.
J Cutan Pathol ; 51(8): 576-582, 2024 Aug.
Article en En | MEDLINE | ID: mdl-38666479
ABSTRACT
Melanoma's rare capacity to undergo heterologous differentiation can create significant diagnostic challenges. The molecular mechanisms underlying this phenomenon are not well understood. We present an unusual case of subungual melanoma exhibiting extensive cartilaginous differentiation and provide insights into its molecular and cytogenomic features. Histopathologically, the tumor was predominantly composed of nodules of malignant cartilage in association with a smaller population of nested epithelioid to rhabdoid cells. Immunohistochemically, the tumor cells in both components were positive for S100, SOX10, and PRAME, and were negative for Melan-A and HMB-45. Molecular analysis by whole exome DNA sequence did not detect any pathogenic variants in genes commonly implicated in melanoma. Additional analysis by SNP chromosomal microarray revealed a complex genome characterized by numerous chromosomal losses and gains, including a homozygous deletion of the CDKN2A locus and a heterozygous deletion of the locus containing EXT2, a tumor suppressor implicated in hereditary multiple osteochondromas and secondary chondrosarcomas. This case underscores the importance of recognizing cartilaginous differentiation as a rare manifestation of melanoma, particularly at subungual sites, and suggests that at least some of these melanomas may be driven by non-canonical molecular pathways.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Cutáneas / Melanoma / Enfermedades de la Uña Límite: Female / Humans / Male Idioma: En Revista: J Cutan Pathol Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Cutáneas / Melanoma / Enfermedades de la Uña Límite: Female / Humans / Male Idioma: En Revista: J Cutan Pathol Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos