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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引用次数: 0

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。

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

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

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

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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