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

Author:

Hasegawa Eiko1,Sawa Naoki1,Hoshino Junichi12,Suwabe Tatsuya1,Hayami Noriko1,Yamanouchi Masayuki1,Sekine Akinari1,Hiramatsu Rikako1,Imafuku Aya1,Kawada Masahiro1,Ubara Yoshifumi12,Imamura Tsunao3,Takaichi Kenmei12

Affiliation:

1. Nephrology Center, Toranomon Hospital, Japan

2. Okinaka Memorial Institute for Medical Research, Japan

3. Department of Gastroenterology, Toranomon Hospital, Japan

Publisher

Japanese Society of Internal Medicine

Subject

General Medicine,Internal Medicine

Reference22 articles.

1. 1. Comfort MW, Gary HK, Dahlin DC, Whitesell FB Jr. Polycystic disease of the liver: a study of 24 cases. Gastroenterology 20: 60-78, 1952.

2. 2. Caroli J, Soupault R, Kossakowski J, Plocker L, Paradowska M. La dilatation polykystique congénitale des voies bilaires intra-hepatiques. Essai de classification. Sem Hop Paris 34: 128-135, 1958 (in French).

3. 3. Berenuger J, Olaso V, Rayón M, et al. Dilatacion congenital no obstructive de los condoctos biliares intrahepaticos segmentarios (enfermedad de Caroli) Presentacion de una observacion y revision de la literature. Rev Clin Esp 140: 567-577, 1976 (in Spanish).

4. 4. Jordon D, Harpaz N, Thung S. Caroli's disease and adult polycystic kidney disease: a rarely recognized association. Liver 9: 30-35, 1989.

5. 5. Mousson C, Rabec M, Cercueil JP, Virot JS, Hillon P, Rifle G. Caroli's disease and autosomal dominant polycystic kidney disease: a rare association? Nephrol Dial Transplant 12: 1481-1483, 1997.

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