| Literature DB >> 29554022 |
Shayan Sengupta1, Angela C Weyand2, Santhosh A Upadhyaya3, Yi-Mi Wu4, Dan R Robinson5, Rajen J Mody2.
Abstract
Germline mutation of BRCA-associated protein-1 has been implicated in the development of tumor predisposition syndrome and high risk for malignant mesothelioma, lung adenocarcinoma, uveal melanoma, and cutaneous melanoma. Here, we present the case of a patient with recurrent metastatic melanoma who was found to have germline BAP1 and somatic BRAF mutation by clinical genomic sequencing. Detection of a germline mutation prompted screening for other cancers and surveillance in family members. Prospective integrative sequencing for pediatric cancer patients may identify pathogenic germline mutations and may improve outcomes and treatment-related morbidity by early diagnosis of malignancy.Entities:
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Year: 2019 PMID: 29554022 PMCID: PMC6139285 DOI: 10.1097/MPH.0000000000001122
Source DB: PubMed Journal: J Pediatr Hematol Oncol ISSN: 1077-4114 Impact factor: 1.289