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胆道闭锁行肝门空肠吻合术后迟发性胆管炎和Roux袢梗阻

Late-presenting cholangitis and Roux loop obstruction after Kasai portoenterostomy for biliary atresia.

作者信息

Houben Chris, Phelan Sean, Davenport Mark

机构信息

The Department of Paediatric Surgery, King's College Hospital, SE5 9RS London, UK.

出版信息

J Pediatr Surg. 2006 Jun;41(6):1159-64. doi: 10.1016/j.jpedsurg.2006.01.066.

DOI:10.1016/j.jpedsurg.2006.01.066
PMID:16769353
Abstract

BACKGROUND/PURPOSE: Late-onset cholangitis is an uncommon complication after the Kasai operation for biliary atresia. Experience with 3 recent patients illustrates appropriate management.

METHODS

Retrospective review of patients with late unexplained deterioration in liver function attributed to cholangitis. All underwent quantitative radioisotope hepatobiliary scans to identify the Roux loop obstruction and confirm postoperative resolution. The role of percutaneous transhepatic cholangiography and computed tomography scanning was reviewed.

RESULTS

Three patients aged 8, 13, and 17 years were identified. All 3 had had a successful Kasai portoenterostomy for type 3 biliary atresia and presented after several virtually trouble-free years with late-onset cholangitis. The radioisotope scans in all 3 patients showed poor tracer uptake by the liver and pooling of the radioisotope at the porta hepatis. Laparotomy confirmed a proximal Roux loop obstruction at the level of the mesocolic window in all. This required mobilization and adhesiolysis and, in 1, correction of an actual stenosis within the wall of the intestine at this level. All patients had normalization of their liver function postoperatively. All are now well and anicteric at a follow-up of 6 to 12 months.

CONCLUSIONS

Long-term survivors of the Kasai portoenterostomy for biliary atresia with immediate deterioration in liver function warrant investigation for possible Roux loop obstruction. Resolution of the obstruction allows preservation of their native liver.

摘要

背景/目的:迟发性胆管炎是胆道闭锁Kasai手术后一种不常见的并发症。近期3例患者的治疗经验说明了合理的处理方法。

方法

回顾性分析因胆管炎导致肝功能不明原因迟发性恶化的患者。所有患者均接受了放射性核素肝胆定量扫描,以确定Roux袢梗阻情况并确认术后梗阻是否解除。对经皮经肝胆管造影和计算机断层扫描的作用进行了评估。

结果

确定了3例患者,年龄分别为8岁、13岁和17岁。所有3例患者均因3型胆道闭锁成功接受了Kasai肝门空肠吻合术,在经历了数年几乎无问题的时期后出现迟发性胆管炎。所有3例患者的放射性核素扫描均显示肝脏对示踪剂摄取不良,放射性核素在肝门处积聚。剖腹手术证实所有患者在结肠系膜窗水平均存在近端Roux袢梗阻。这需要进行游离和粘连松解,其中1例患者还需要纠正该水平肠壁内的实际狭窄。所有患者术后肝功能均恢复正常。在6至12个月的随访中,所有患者目前情况良好,无黄疸。

结论

Kasai肝门空肠吻合术治疗胆道闭锁的长期存活者若出现肝功能立即恶化,需对可能的Roux袢梗阻进行检查。梗阻解除后可保留其自身肝脏。

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