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J Pediatr Hematol Oncol ; 44(3): e751-e755, 2022 Apr 01.
Article in English | MEDLINE | ID: mdl-34224514

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.


Subject(s)
Hemangiosarcoma , Pancreatic Neoplasms , Adolescent , Female , Hemangiosarcoma/genetics , Hemangiosarcoma/pathology , Hemangiosarcoma/surgery , Humans , Pancreas/pathology , Pancreas/surgery , Pancreatectomy , Pancreatic Neoplasms/genetics , Pancreatic Neoplasms/surgery , Pancreaticoduodenectomy , Vascular Endothelial Growth Factor Receptor-2
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