Mirizzi综合征合并胆总管瘘:从无症状胆囊结石发展到手术的观察。

Case Reports in Radiology Pub Date : 2020-01-27 eCollection Date: 2020-01-01 DOI:10.1155/2020/2049525
Hiroyuki Sugo, Yuuki Sekine, Naoki Iwanaga, Shigefumi Neshime, Michio Machida
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引用次数: 0

摘要

尽管有大量关于Mirizzi综合征的报道,但没有一个报道描述其从单纯性胆囊结石发展的过程。我们报告一例极为罕见的Mirizzi综合征病例,在该病例中,我们可以观察到从无症状胆囊结石到4年后不可避免的手术干预,胆囊胆瘘的发展过程。一名68岁女性因右上腹疼痛来我院就诊。4年前,她被诊断为无症状胆囊结石。诊断性腹部计算机断层扫描(CT)显示1.9厘米不透射线的结石,此后,患者仅通过影像学监测。入院前6个月CT显示胆囊结石压迫肝总管,但患者无症状。入院时,腹部CT显示胆囊结石阻塞胆总管并扩张肝内管。内镜逆行胆管造影示胆总管与胆囊管汇合处圆形充盈缺损;因此,根据Csendes分型,将患者归类为Mirizzi综合征III型。术中发现一胆管瘘累及胆管总周长的三分之二。
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 with Cholecystobiliary Fistula: Observation of Development from Asymptomatic Cholecystolithiasis to Surgery.

Mirizzi Syndrome with Cholecystobiliary Fistula: Observation of Development from Asymptomatic Cholecystolithiasis to Surgery.

Mirizzi Syndrome with Cholecystobiliary Fistula: Observation of Development from Asymptomatic Cholecystolithiasis to Surgery.

Mirizzi Syndrome with Cholecystobiliary Fistula: Observation of Development from Asymptomatic Cholecystolithiasis to Surgery.

Despite a considerable number of reports of Mirizzi syndrome, none have described the process of its development from simple cholecystolithiasis. We report an extremely rare case of Mirizzi syndrome in which it was possible to observe the process of development of cholecystobiliary fistula from asymptomatic cholecystolithiasis until unavoidable surgical intervention 4 years later. A 68-year-old woman presented at our hospital with right upper quadrant pain. She had been diagnosed as having asymptomatic cholecystolithiasis 4 years previously. Diagnostic abdominal computed tomography (CT) had revealed a 1.9 cm radiopaque stone, and thereafter, the patient had been monitored by imaging alone. CT conducted 6 months before the present admission revealed that the gallbladder stone was compressing the common hepatic duct, although the patient remained asymptomatic. On admission, abdominal CT showed that the gallbladder stone was obstructing the common bile duct with dilatation of the intrahepatic duct. Endoscopic retrograde cholangiopancreatography revealed a round filling defect at the confluence of the common bile duct and the image of the cystic duct; therefore, the patient was categorized as having Mirizzi syndrome type III, according to the Csendes classification. Intraoperative findings revealed a cholecystobiliary fistula involving up to two-thirds of the circumference of the common bile duct.

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