Kakkos S K, Vagenas C A, Spiliotis J D, Thomopoulos C, Androulakis J A
Department of Surgery, University of Patras Medical School, Greece.
Hepatogastroenterology. 1998 Nov-Dec;45(24):2410-2.
A rare case of the ductectatic variant of mucinous pancreatic cystadenocarcinoma in a 64 year-old man, presenting with painless obstructive jaundice, is reported. CT scan revealed a multicystic lesion of the pancreatic head, which caused biliary obstruction. Endoscopic retrograde pancreatography (ERP) revealed the characteristic grapelike cluster pattern of pancreatic ductectatic neoplasms. Pancreaticoduodenectomy was then successfully performed. Pancreatic ductectatic mucinous cystadenocarcinoma is a rare entity, presenting, usually, with obstructive pancreatitis, and is histologically indistinguishable from the classic malignant mucinous cystic neoplasm. ERP is the diagnostic method of choice and should be performed in any case of susceptible pancreatic lesions.
报道了一例64岁男性黏液性胰腺囊腺癌导管扩张型罕见病例,该患者表现为无痛性梗阻性黄疸。CT扫描显示胰头有一个多囊性病变,导致胆道梗阻。内镜逆行胰胆管造影(ERP)显示了胰腺导管扩张性肿瘤特征性的葡萄串样簇状形态。随后成功实施了胰十二指肠切除术。胰腺导管扩张性黏液性囊腺癌是一种罕见的疾病,通常表现为梗阻性胰腺炎,在组织学上与经典的恶性黏液性囊性肿瘤无法区分。ERP是首选的诊断方法,对于任何可疑的胰腺病变都应进行该检查。