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肝总管良性梗阻(Mirizzi综合征):诊断与手术治疗

Benign obstruction of the common hepatic duct (Mirizzi syndrome): diagnosis and operative management.

作者信息

Waisberg Jaques, Corona Adriano, de Abreu Isaac Walker, Farah José Francisco de Matos, Lupinacci Renato Arioni, Goffi Fábio Schmidt

机构信息

General Surgery Department, Hospital do Servidor Público Estadual de São Paulo Francisco Morato de Oliveira, São Paulo, SP, Brazil.

出版信息

Arq Gastroenterol. 2005 Jan-Mar;42(1):13-8. doi: 10.1590/s0004-28032005000100005. Epub 2005 Jun 22.

Abstract

BACKGROUND

Mirizzi syndrome is a rare complication of prolonged cholelithiasis, characterized by narrowing of the common hepatic duct due to mechanical compression and/or inflammation due to biliary calculus impacted in the infundibula of the gallbladder or in the cystic duct.

OBJECTIVES

To describe a series of eight consecutive patients with Mirizzi syndrome, at a single institution, submitted to surgical treatment and to comment on their aspects with emphasis on the diagnosis and treatment.

METHODS

Four women and four men, with a mean age of 61.6 years (42 to 82 years), presenting Mirizzi syndrome were operated between 1997 and 2003. The following items were evaluated: clinical presentation, laboratory results, preoperative evaluation, operative findings, presence of choledocholithiasis, type of Mirizzi syndrome according to the classification by Csendes, choice of operative procedures, and complications.

RESULTS

The most frequent symptoms were abdominal pain (87.5%) and jaundice (87.5%). All the patients presented altered hepatic function tests. The diagnosis of Mirizzi syndrome was intra-operative in seven (87.5%) patients, and preoperative in one (12.5%). Cholecystocholedochal fistula associated with choledocholithiasis was observed in three (37.5%) cases. Mirizzi syndrome was classified as Csendes type I in five (62.5%) patients, type II in one (12.5%), type III in one (12,5%) and type IV in another (12.5%). Cholecystectomy, as an isolated surgical procedure, was performed in four (50.0%) patients. One (12.5%) patient was submitted to partial cholecystectomy and closure of the fistulous orifice with the central part of the infundibula. Two (25.0%) patients were submitted to cholecystectomy and side-to-side choledochoduodenostomy and another (12.5%) to side-to-side choledochoduodenostomy remaining the gallbladder in situ. Seven (87.5%) patients had an uneventful recovery and were discharged in good conditions. One (12.5%) patient presented a postoperative sepsis due to a sub-hepatic abscess, and was reoperated. There was no operative mortality.

CONCLUSION

The preoperative diagnosis of Mirizzi syndrome is difficult and an awarded suspicion is necessary to avoid lesions of the biliary tree. The problem may only become evident during the operation due to firm adherences around Calot's triangle. The success of the treatment is related to a precocious recognition of the condition, even at the time of surgery, and adapting the management considering to the individual characteristics of each case.

摘要

背景

Mirizzi综合征是长期胆石症的一种罕见并发症,其特征是由于胆囊漏斗部或胆囊管内的胆结石机械性压迫和/或炎症导致肝总管狭窄。

目的

描述在单一机构连续收治的8例接受手术治疗的Mirizzi综合征患者,并重点对其诊断和治疗方面进行评论。

方法

1997年至2003年间,对4名女性和4名男性、平均年龄61.6岁(42至82岁)的Mirizzi综合征患者进行了手术。评估了以下项目:临床表现、实验室检查结果、术前评估、手术发现、胆总管结石的存在情况、根据Csendes分类的Mirizzi综合征类型、手术方式的选择及并发症。

结果

最常见的症状是腹痛(87.5%)和黄疸(87.5%)。所有患者肝功能检查均有异常。7例(87.5%)患者在术中诊断为Mirizzi综合征,1例(12.5%)为术前诊断。3例(37.5%)患者观察到合并胆总管结石的胆囊胆总管瘘。5例(62.5%)患者的Mirizzi综合征被分类为Csendes I型,1例(12.5%)为II型,1例(12.5%)为III型,另1例(12.5%)为IV型。4例(50.0%)患者单独进行了胆囊切除术。1例(12.5%)患者接受了部分胆囊切除术,并用漏斗部中央部分封闭瘘口。2例(25.0%)患者接受了胆囊切除术和胆总管十二指肠侧侧吻合术,另1例(12.5%)接受了胆总管十二指肠侧侧吻合术,胆囊原位保留。7例(87.5%)患者恢复顺利,状况良好出院。1例(12.5%)患者因肝下脓肿出现术后败血症,再次接受手术。无手术死亡病例。

结论

Mirizzi综合征的术前诊断困难,必须高度怀疑以避免胆道树损伤。由于胆囊三角周围粘连紧密,该问题可能仅在手术过程中才变得明显。治疗的成功与对病情的早期识别有关,即使在手术时也是如此,并根据每个病例的个体特征调整治疗方案。

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