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Autoimmune pancreatitis with atypical imaging findings that mimicked an endocrine tumor
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作者 cindy Neuzillet céline lepère +6 位作者 Mostafa El Hajjam Laurent Palazzo Monique Fabre Hajer Turki Pascal Hammel Philippe Rougier Emmanuel Mitry 《World Journal of Gastroenterology》 SCIE CAS CSCD 2010年第23期2954-2958,共5页
Autoimmune pancreatitis(AIP) is a rare cause of recurrent acute pancreatitis or chronic pancreatitis in middleaged patients,and is characterised by a marked infiltration of lymphocytes and plasma cells in pancreatic t... Autoimmune pancreatitis(AIP) is a rare cause of recurrent acute pancreatitis or chronic pancreatitis in middleaged patients,and is characterised by a marked infiltration of lymphocytes and plasma cells in pancreatic tissue.Diagnosis of focal forms can be diff icult as AIP may mimic pancreatic adenocarcinoma.Pediatric cases of AIP are exceptional.We report the case of a 15-yearold girl who had a focal AIP and associated cholangitis,with a very unusual vascularized mass that mimicked a pancreatic endocrine tumor.The diagnosis was obtained by a pancreatic biopsy,thus avoiding surgical resection,and all the clinical,biological and radiological abnormalities resolved after steroid therapy with 6 mo of follow-up. 展开更多
关键词 PANCREAS Autoimmune pancreatitis ADOLESCENT Endocrine tumor BIOPSY
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