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Spontaneous perforation of the biliary tract and portal vein thrombosis in infancy

机译:婴儿期自发性胆道穿孔和门静脉血栓形成

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摘要

Spontaneous biliary perforation (SBP) is an uncommon cause of surgical jaundice in the first few weeks of life and is characterised by the occurrence of a punched-out defect in the bile duct, typically where the cystic duct joins the common hepatic duct. In most cases the site occurs anteriorly and bile leaks into the general peritoneal cavity. We now describe two cases of SBP where the perforation occurred posteriorly, limiting the leak and resulting in delayed recognition. Surgical management in both cases consisted of hepaticojejunostomy-en-Roux. Both cases were complicated, although not immediately, by portal vein thrombosis and one by chylous ascites. Posterior SBP, presumably due to their intimate anatomical relation with the portal vein, seem predisposed to such complications.
机译:自发性胆道穿孔(SBP)在生命的最初几周内很少发生外科手术性黄疸,其特征是胆管中出现穿孔缺损,通常是胆囊管与肝总管相连的地方。在大多数情况下,该部位发生在前部,并且胆汁泄漏到腹膜腔内。现在,我们描述了两个SBP案例,其中穿孔发生在后面,限制了渗漏并导致识别延迟。两种情况的手术处理均包括肝空肠吻合术。两种情况虽然不是立即发生,但门静脉血栓形成比较复杂,而乳糜性腹水则很复杂。后SBP,可能是由于其与门静脉的紧密解剖关系,似乎易患此类并发症。

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