首页> 外文期刊>Journal of Hepatology: The Journal of the European Association for the Study of the Liver >Biliary obstruction caused by portal cavernoma: a study of 8 cases.
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Biliary obstruction caused by portal cavernoma: a study of 8 cases.

机译:门孔瘤瘤引起的胆道阻塞:8例研究。

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BACKGROUND/AIMS: Biliary obstruction secondary to portal cavernoma is a rare and little-known entity. From 1985 to 1994, we observed eight cases of portal cavernoma compressing the biliary tract. We report here the features of biliary involvement in these cases of portal cavernoma including the circumstances of diagnosis, biliary tract morphology, liver pathology and the efficiency of various treatments. METHODS AND RESULTS: The causes of portal vein obstruction were portal vein thrombosis in one case, peritonitis in another, omphalitis in two cases, portal vein catheterization in one case and unknown in two cases. The portal cavernoma was revealed through esophageal varices ruptures in four patients. The mean time from portal cavernoma diagnosis to biliary involvement was 8 years (range 0-21). Six patients had acute cholangitis, one of whom revealed portal vein obstruction. All the patients had abnormal liver function tests. Imaging techniques (transparietal abdominal ultrasonography and abdominal computed tomography scan [n = 8], endosonography [n = 5] and endoscopic retrograde cholangiography [n = 7]) showed in all cases an extraluminal obstacle, laminating the common bile duct. Pathologic examination of the liver showed secondary biliary cirrhosis in one patient, periportal and perisinusoidal fibrosis in another and no abnormalities in three other cases. Three patients were treated by endoscopic sphincterotomy but cholangitis persisted in two cases, leading to death in one. One patient who underwent a splenorenal shunt was symptom-free 60 months after surgery. Balloon endoscopic dilatation of the common bile duct, performed in one case, led to normalization of liver biological tests. The patients with abnormal liver pathology were treated by propranolol and ursodesoxycholic acid. No complication had occurred after 6 and 24 months of follow-up. CONCLUSIONS: In conclusion, eliminating biliary obstruction seems to be essential in providing the best change of survival for patients when biliary obstruction becomes symptomatic. In cases of abnormal liver pathology, associating propranolol with ursodesoxycholic acid would seem to be useful.
机译:背景/目的:胆道阻塞到门野窦瘤是一种罕见的和鲜为人知的实体。从1985年到1994年,我们观察了八个案例的门穴探空血管瘤瘤。我们在此报告胆道参与这些门穴血管瘤病例的特征,包括诊断情况,胆道形态,肝脏病理学和各种治疗的效率。方法和结果:门静脉阻塞的原因是一种病态静脉血栓形成,在一种情况下,另一个腹膜炎,两种情况下,门静脉导管插入术中的两种情况未知。通过食管静脉曲张在四名患者中破裂揭示了门户气囊瘤。从门穴探空瘤对胆道参与的平均时间为8年(范围0-21)。六名患者患有急性胆管炎,其中一个人揭示了门静脉阻塞。所有患者均有异常的肝功能测试。成像技术(临时腹部超声和腹部计算断层摄影扫描[n = 8],内窥镜检查[n = 5]和内窥镜逆行胆管造影[n = 7])在所有情况下都显示出普通壳体,层压胆管。肝脏病理检查在另一种患者,围绕围绕和嗜来自Perisinupoideral纤维化的继发性胆汁肝硬化,另外三种情况下没有异常。三名患者通过内窥镜晶状体切开术治疗,但胆管炎在两种情况下持续存在,导致死亡。一个接受脾脏分流器的患者在手术后60个月出现症状。球囊内镜膨胀胆管导管在一种情况下进行,导致肝脏生物试验的正常化。肝脏病理异常患者由普萘洛尔和福科糖酸酸治疗。后续6和24个月后没有发生任何并发症。结论:总之,消除胆管梗阻似乎在胆道阻塞变得症状时为患者提供最佳的存活变化至关重要。在异常肝脏病理学的情况下,将丙烯醇与熊毒性胆酸似乎是有用的。

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