A Case of Hepatic Cyst Infection in a Hemodialysis Patient with Autosomal Dominant Polycystic Kidney Disease Complicated by Non-symptomatic Caroli Disease.

Ayaka Hane, Tatsuya Suwabe, Yuki Oba, Shigekazu Kurihara, Hiroki Mizuno, Hisashi Kamido, Hisashi Sugimoto, Noriko Inoue, Akinari Sekine, Masayuki Yamanouchi, Kiho Tanaka, Eiko Hasegawa, Takehiko Wada, Naoya Mirisada, Kandai Nozu, Naoki Sawa, Yoshifumi Ubara
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Abstract

An 84-year-old woman undergoing hemodialysis for autosomal dominant polycystic kidney disease (ADPKD) was admitted for refractory hepatic cyst infection. Magnetic resonance cholangiopancreatography and contrast-enhanced computed tomography revealed a concurrent complication of Caroli disease, diagnosed by cystic dilatation of the intrahepatic bile duct and a central dot sign in the vicinity of the infected liver cyst. However, there was no traffic between the infected liver cyst and dilated bile duct, and the cyst drainage procedure was curative. In cases where both diseases were combined, it was suggested that two infections, cyst and biliary tract infections, could occur.

常染色体显性多囊肾病合并无症状Caroli病的血液透析患者肝囊肿感染1例
一名84岁妇女因常染色体显性多囊肾病(ADPKD)接受血液透析,因难治性肝囊肿感染入院。磁共振胆管造影和增强计算机断层扫描显示Caroli病并发并发症,通过肝内胆管囊性扩张和受感染肝囊肿附近的中心点征诊断。然而,感染的肝囊肿和扩张的胆管之间没有交通,囊肿引流手术是治愈的。在两种疾病合并的情况下,建议两种感染,囊肿和胆道感染,可能发生。
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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