Description of the disease * EnglishPolish Pobierz sekcję do PDF Definicja A rare pancreatic disease characterized by a most commonly single, unilocular, thin-walled cystic lesion which may be located anywhere within the pancreas (but is more frequently found in the body and tail) and does not communicate with the pancreatic ductal system. Patients may be asymptomatic or present with signs and symptoms of gastrointestinal or biliary obstruction, or pancreatitis. The condition can be isolated or occur in association with other anomalies (such as von Hippel-Lindau disease or polycystic kidney disease). Disease data Klasyfikacja Morphological anomaly Synonimy Neonatal congenital pancreatic cyst Noworodkowa wrodzona torbiel trzustki Prawdziwa wrodzona torbiel trzustki True congenital pancreatic cyst Kod ORPHA 313906 Kod OMIM - Kod ICD10 Q45.2 Kod ICD11 LB21.Y *Soruce Extended description of the disease Pobierz sekcję do PDF No additional description. Orphanet - interntowa baza danych dotyczących rzadkich chorób i sierochych leków. ©INSERM 1999 - Dostępna na stronie www.orphanet.pl