| Literature DB >> 30801340 |
Phyu P Aung1, Priyadharsini Nagarajan1, Michael T Tetzlaff2, Jonathan L Curry2,3, Guilin Tang4, Zied Abdullaev5, Svetlana D Pack6, Doina Ivan2,3, Victor G Prieto7,8, Carlos A Torres-Cabala9.
Abstract
The presence of multiple BAP1-negative melanocytic neoplasms is a hallmark of familial cancer susceptibility syndrome caused by germline mutations in BAP1. Melanocytic tumors lacking BAP1 expression may also present as sporadic lesions in patients lacking a germline BAP1 mutation. Here, we report histomorphologic and clinical characteristics of cutaneous melanomas with loss of BAP1 expression in 4 patients with no known history of BAP1-associated cancer susceptibility syndrome. The lesions were nodular melanomas composed predominantly of intradermal large epithelioid (Spitzoid) melanocytes with nuclear pseudoinclusions as well as scattered multinucleated cells, arising in association with a typical intradermal nevus. Of the 4 patients, only 1 had recurrence. This patient had multiple recurrences with in-transit and regional lymph node metastases. To the best of our knowledge, this is the first reported series of cutaneous melanomas with loss of BAP1 expression arising in patients without a family history of cancer.Entities:
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Year: 2019 PMID: 30801340 PMCID: PMC8191382 DOI: 10.1097/DAD.0000000000001217
Source DB: PubMed Journal: Am J Dermatopathol ISSN: 0193-1091 Impact factor: 1.533