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门静脉海绵样变性所致胆道梗阻:8例研究

Biliary obstruction caused by portal cavernoma: a study of 8 cases.

作者信息

Perlemuter G, Béjanin H, Fritsch J, Prat F, Gaudric M, Chaussade S, Buffet C

机构信息

Service des Maladies du Foie et de l'Appareil Digestif, Hôpital de Bicêtre, Kremlin Bicêtre, France.

出版信息

J Hepatol. 1996 Jul;25(1):58-63. doi: 10.1016/s0168-8278(96)80328-x.

Abstract

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.

摘要

背景/目的:门静脉海绵样变继发胆道梗阻是一种罕见且鲜为人知的疾病。1985年至1994年期间,我们观察到8例门静脉海绵样变压迫胆道的病例。在此,我们报告这些门静脉海绵样变病例中胆道受累的特征,包括诊断情况、胆道形态、肝脏病理以及各种治疗方法的疗效。

方法与结果

门静脉梗阻的原因分别为:1例门静脉血栓形成、1例腹膜炎、2例脐炎、1例门静脉插管,2例原因不明。4例患者通过食管静脉曲张破裂发现门静脉海绵样变。从门静脉海绵样变诊断到胆道受累的平均时间为8年(范围0 - 21年)。6例患者发生急性胆管炎,其中1例显示门静脉梗阻。所有患者肝功能检查均异常。影像学检查(经腹壁超声和腹部计算机断层扫描[n = 8]、内镜超声[n = 5]和内镜逆行胆管造影[n = 7])在所有病例中均显示管腔外有压迫胆总管的障碍物。肝脏病理检查显示,1例患者为继发性胆汁性肝硬化,另1例为汇管区和窦周纤维化,其他3例无异常。3例患者接受了内镜括约肌切开术,但2例胆管炎持续存在,其中1例死亡。1例行脾肾分流术的患者术后60个月无症状。1例行胆总管球囊内镜扩张术的患者肝脏生化检查恢复正常。肝脏病理异常的患者接受了普萘洛尔和熊去氧胆酸治疗。随访6个月和24个月后均未发生并发症。

结论

总之,当胆道梗阻出现症状时,消除胆道梗阻似乎是为患者提供最佳生存机会的关键。对于肝脏病理异常的病例,联合使用普萘洛尔和熊去氧胆酸似乎是有效的。

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