Combined Liver and Kidney Transplant in a Patient with Budd-Chiari Syndrome Secondary to Autosomal Dominant Polycystic Kidney Disease Associated with Polycystic Liver Disease: Report of a Case with a 9-Year Follow-Up

Polycystic liver disease (PLD) is a hereditary disease inherited by autosomal dominant trait that occurs as a frequent extrarenal manifestation of autosomal dominant polycystic kidney disease (ADPKD). We report a case of a 59-year-old woman diagnosed with ADPKD associated with PLD. End-stage chronic...

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Detalles Bibliográficos
Autores principales: Ramírez de la Piscina, Patricia, Duca, Ileana, Estrada, Silvia, Calderón, Rosario, Ganchegui, Idoia, Campos, Amaia, Spicakova, Katerina, Urtasun, Leire, Salvador, Marta, Delgado, Elvira, Bengoa, Raquel, García-Campos, Francisco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4058590/
https://www.ncbi.nlm.nih.gov/pubmed/24987537
http://dx.doi.org/10.1155/2014/585291

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4058590/
https://www.ncbi.nlm.nih.gov/pubmed/24987537
http://dx.doi.org/10.1155/2014/585291

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