| Literature DB >> 30945443 |
Aline Baltres1, Aicha Salhi2, Aurelie Houlier1,3, Daniel Pissaloux1,3, Franck Tirode3, Véronique Haddad1, Marie Karanian1,3, Salim Ysmail-Dahlouk4, Fatma Boukendakdji5, Djazia Dahlouk5, Fateh Allaoua6, Marzak Metref6, Assya Djeridane7, Sylvie Fraitag8, Arnaud de la Fouchardière1,3.
Abstract
A girl, born with a posterior lumbosacral giant congenital nevus, developed a central nodule that expanded over a period of 14 months into a 10-cm pedunculated mass. Histological analysis of the mass revealed melanoma of myxoid, small round-cell type with areas of rhabdomyosarcomatous transformation confirmed by immunohistochemistry. RNA sequencing identified an in-frame SASS6(e14)-RAF1(e8) fusion in both components and the nevus. A RAF1 FISH break-apart test found a balanced rearrangement pattern in the nevus and an unbalanced pattern in the malignant areas. Wild-type status of NRAS and BRAF was confirmed by NGS techniques. The array-CGH profile displayed copy number alterations commonly found in rhabdomyosarcomas. Despite intensive treatment, widespread metastatic evolution of the melanomatous component was observed.Entities:
Keywords: RAF1 fusion; congenital melanoma; giant congenital nevus; rhabdomyosarcomatous differentiation; small-cell melanoma
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Year: 2019 PMID: 30945443 DOI: 10.1111/pcmr.12785
Source DB: PubMed Journal: Pigment Cell Melanoma Res ISSN: 1755-1471 Impact factor: 4.693