| Literature DB >> 34224514 |
Richard S Whitlock1,2, Kingsley Ebare3, Lily S Cheng1,2, Douglas S Fishman4, Joseph L Mills5, HaiThuy N Nguyen6, Jed G Nuchtern1,2, Wenly Ruan4, Valeria E Smith7, Kalyani A Patel3, Kevin E Fisher3, Sanjeev A Vasudevan1,2.
Abstract
Pancreatic angiosarcoma is an exceedingly rare malignancy accounting for <1% of pancreatic neoplasms. A very limited number of pancreatic angiosarcomas have been reported in the literature without any cases described in children. We present the case of a 17-year-old female diagnosed with angiosarcoma of the pancreas following pancreaticoduodenectomy for a pancreatic mass, initially presumed to be a solid pseudopapillary neoplasm of the pancreas. The angiosarcoma was found to have a novel activating internal tandem duplication in the KDR gene (KDR-internal tandem duplication). We discuss the current literature on this disease process. This is the first reported case of pancreatic angiosarcoma in a pediatric patient and the first with an activating KDR-internal tandem duplication.Entities:
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Year: 2022 PMID: 34224514 DOI: 10.1097/MPH.0000000000002248
Source DB: PubMed Journal: J Pediatr Hematol Oncol ISSN: 1077-4114 Impact factor: 1.170