| Literature DB >> 30803559 |
Jianling Ji1, Fariba Navid2, Mathew C Hiemenz3, Maki Kaneko4, Shengmei Zhou3, Sulagna C Saitta3, Jaclyn A Biegel3.
Abstract
Germline pathogenic variants in CBL are associated with an autosomal dominant RASopathy and an increased risk for malignancies, particularly juvenile myelomonocytic leukemia. Herein, we describe a patient with clinical features of a Noonan-spectrum disorder who developed embryonal rhabdomyosarcoma of the bladder at age two years. Tumor analysis using the OncoKids® cancer panel revealed a CBL pathogenic variant: NM_005188.3:c.1100A>C (p.Gln367Pro). Sanger sequencing of peripheral blood DNA confirmed a de novo heterozygous germline variant. This is the first report of embryonal rhabdomyosarcoma in association with a germline CBL pathogenic variant, further broadening the CBL cancer predisposition spectrum. Published by Elsevier Inc.Entities:
Keywords: CBL; Cancer predisposition; Embryonal rhabdomyosarcoma; RASopathy
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Year: 2018 PMID: 30803559 DOI: 10.1016/j.cancergen.2018.12.006
Source DB: PubMed Journal: Cancer Genet