Mirizzi综合征并发4型胆囊胆瘘至右肝管。

Christina M Stuart, Madeline G Huey, Christian V Ghincea, Fredric M Pieracci, Magdalene Brooke
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摘要

Mirizzi综合征是一种罕见的长期慢性胆囊炎并发症,其特征是肝总管的外源性压迫,可能发展为胆管瘘。我们在此报告一位38岁的女性病患,因急性胆囊炎及胆总管结石而行腹腔镜胆囊切除术及术中胆道造影。术中发现患者有Mirizzi综合征并发右肝管胆管瘘。成功切除胆囊,清除胆结石,并使用输尿管支架进行重建。患者于术后2日出院,常规随访情况良好。最后,Mirizzi综合征是一种罕见的临床疾病,术前检查时需要仔细考虑,术中遇到解剖异常时高度怀疑。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Mirizzi syndrome complicated by type IV cholecystobiliary fistula to the right hepatic duct.

Mirizzi syndrome is a rare complication of long-term chronic cholecystitis, characterized by extrinsic compression of the common hepatic duct that may progress to development of cholecystobiliary fistula. Here we report a case of a 38-year-old female patient who underwent laparoscopic cholecystectomy with intraoperative cholangiogram for acute cholecystitis and choledocholithiasis. Intraoperatively, the patient was found to have a Mirizzi syndrome complicated by cholecystobiliary fistula to the right hepatic duct. The gallbladder was successfully removed, cholelithiasis cleared and a ureteral stent was used in reconstruction. The patient was discharged on postoperative two and was doing well on routine follow-up. Ultimately, Mirizzi syndrome is a rare clinical entity that requires careful consideration during preoperative workup and a high suspicion when abnormal anatomy is encountered intraoperatively.

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