Lilly J R, Stellin G P, Karrer F M
J Pediatr Surg. 1985 Aug;20(4):449-51. doi: 10.1016/s0022-3468(85)80239-6.
Four patients had the characteristic features of choledochal cyst except for the cystic component. All patients had stenosis of the distal common bile duct, a "long common channel" secondary to a proximal junction of the common bile and pancreatic ducts, cholecystitis and the classic pathological microscopic features of choledochal cyst in the wall of the common bile duct. Three children had coexisting intrahepatic duct cysts and/or stenosis and one had intrahepatic choledocholithiasis. The clinical presentations were cholangitis (2), pancreatitis (1) and biliary obstruction (1). In all cases the common bile duct was resected and biliary reconstruction was carried out by choledochojejunostomy (Roux-en-Y). Morbidity was minor except in one patient with ductal disease extending far into the intrahepatic ducts. This child developed an anastomotic stricture requiring revision of the anastomosis and long-term "U" tube stenting. Forme fruste choledochal cyst appears to be another variation in the spectrum of pancreaticobiliary malformations of choledochal cyst. Treatment is identical, that is, excision of all malformed ductal tissue.
4例患者除无囊性成分外,具有胆总管囊肿的特征性表现。所有患者均存在胆总管远端狭窄、因胆总管与胰管近端汇合导致的“长共同通道”、胆囊炎以及胆总管壁上胆总管囊肿的典型病理微观特征。3例儿童并存肝内胆管囊肿和/或狭窄,1例有肝内胆管结石。临床表现为胆管炎(2例)、胰腺炎(1例)和胆道梗阻(1例)。所有病例均行胆总管切除,并通过胆总管空肠吻合术(Roux-en-Y)进行胆道重建。除1例胆管疾病延伸至肝内胆管较远部位的患者外,其他患者的并发症均较轻微。该患儿出现吻合口狭窄,需要对吻合口进行修复并长期置入“U”形管支架。胆总管囊肿的不完全型似乎是胆总管囊肿胰胆管畸形谱系中的另一种变异。治疗方法相同,即切除所有畸形的导管组织。