Jung M, Pimentel F, Winter J, Doertenbach J
Abteilung für Gastroenterologie, Johann-Wolfgang-Goethe-Universität Frankfurt/Main.
Z Gastroenterol. 1993 Feb;31(2):147-50.
Congenital abnormalities of the distal bile and pancreatic duct occur predominantly as a long common channel. A common channel of more than 15 mm is considered abnormal, since the length allows a reflux of pancreatic secretion into the bile duct and vice versa. The very rare occurrence of a long common channel syndrome in adults has been observed in two female patients (24 and 58 years old). Both presented cholangitis and/or pancreatitis. Diagnosis was established by ERCP. The definitive therapy in both cases was hepatico-jejunal anastomosis which improved symptoms in both patients. Endoscopic sphincterotomy is unsatisfactory since it does not cut the entire common channel. The rare etiology of a long common channel in patients with cholangitis and pancreatitis is safely verified by ERCP and safely cured by surgical intervention.
远端胆管和胰管的先天性异常主要表现为长的共同通道。超过15毫米的共同通道被认为是异常的,因为这样的长度会使胰液反流至胆管,反之亦然。在两名成年女性患者(分别为24岁和58岁)中观察到了非常罕见的成人长共同通道综合征。两人均表现为胆管炎和/或胰腺炎。通过内镜逆行胰胆管造影术(ERCP)确诊。两例患者的确定性治疗均为肝空肠吻合术,术后症状均有改善。内镜括约肌切开术并不理想,因为它不能切断整个共同通道。通过ERCP可安全地证实胆管炎和胰腺炎患者长共同通道的罕见病因,并通过手术干预安全治愈。