Autosomal dominant polycystic kidney disease ADPKD is a rare disorder, characterized by multiple macroscopic liver and kidney cysts. Isolated Liver transplantation or combined with kidney is a treatment option for these patients with regards to complications arising in hepatic and kidney cysts that are not controlled by other procedures
Liver or combined liver-kidney transplantation for autosomal dominant polycystic kidney disease / D'Amico, G.; Di Benedetto, F.; Tarantino, G.; De Ruvo, N.; Cautero, N.; Montalti, R.; Guerrini, G. P.; Ballarin, R.; Spaggiari, M.; Baisi, B.; Cappelli, G.; Gerunda, G. E.. - In: LIVER TRANSPLANTATION. - ISSN 1527-6465. - 16:6(2010), pp. S242-S243. (Intervento presentato al convegno The International Liver Transplantation Society 16th Annual International Congress tenutosi a Hong Kong, China nel 16-19 Giugno 2010).
Liver or combined liver-kidney transplantation for autosomal dominant polycystic kidney disease
F. Di Benedetto;G. Cappelli
Membro del Collaboration Group
;G. E. Gerunda
2010
Abstract
Autosomal dominant polycystic kidney disease ADPKD is a rare disorder, characterized by multiple macroscopic liver and kidney cysts. Isolated Liver transplantation or combined with kidney is a treatment option for these patients with regards to complications arising in hepatic and kidney cysts that are not controlled by other procedures
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