Opis choroby * EnglishPolish Pobierz sekcję do PDF Definicja Pancreatic endocrine tumor, also known as pancreatic neuroendocrine tumor (PNET), describes a group of endocrine tumors originating in the pancreas that are usually indolent and benign, but may have the potential to be malignant. They can be functional, exhibiting a hormonal hypersecretion syndrome, but can be non-functional presenting with non-specific symptoms and include insulinoma, glucagonoma, VIPoma, somatostatinoma (SSoma), PPoma and Zollinger-Ellison syndrome (ZES, or gastrinoma) and other ectopic hormone producing tumors (such as GRFoma) (see these terms). Dane Klasyfikacja Kategoria Synonimy PNET Pancreatic NET Pancreatic neuroendocrine tumor Well-differentiated NEN of pancreas Well-differentiated neuroendocrine neoplasm of pancreas Well-differentiated pancreatic NEN Well-differentiated pancreatic neuroendocrine neoplasm PNET Pancreatic NET Pancreatic neuroendocrine tumor Well-differentiated NEN of pancreas Well-differentiated neuroendocrine neoplasm of pancreas Well-differentiated pancreatic NEN Well-differentiated pancreatic neuroendocrine neoplasm Kod ORPHA 97253 Kod OMIM - Kod ICD10 E16.8 Kod ICD11 2C10.1 *Źródło Rozszerzony opis choroby Pobierz sekcję do PDF Brak opisu rozszerzonego dla tej choroby. Opracowanie w toku. Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl