Recurrent Cholangitis in a Patient with Autosomal Dominant Polycystic Kidney Disease (ADPKD) and Caroli's Disease

We herein present a rare case of an autosomal dominant polycystic kidney disease (ADPKD) patient with Caroli's disease, a congenital embryonic biliary tree ductal plate abnormality often associated with autosomal recessive polycystic kidney disease. A 76-year-old woman with ADPKD on hemodialysi...

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Dettagli Bibliografici
Pubblicato in:Intern Med
Autori principali: Hasegawa, Eiko, Sawa, Naoki, Hoshino, Junichi, Suwabe, Tatsuya, Hayami, Noriko, Yamanouchi, Masayuki, Sekine, Akinari, Hiramatsu, Rikako, Imafuku, Aya, Kawada, Masahiro, Ubara, Yoshifumi, Imamura, Tsunao, Takaichi, Kenmei
Natura: Artigo
Lingua:Inglês
Pubblicazione: The Japanese Society of Internal Medicine 2016
Soggetti:
Case Report
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC5109570/
https://ncbi.nlm.nih.gov/pubmed/27746440
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