Renal Transplantation in a Patient With Chronic Granulomatous Disease: Case Report

Abstract Chronic granulomatous disease (CGD) is a genetic disease caused by structural mutations in the enzyme NADPH oxidase that results in severe immunodeficiency. End-stage renal disease occurs in this patient population and is attributed to various factors, including infections, amyloidosis, and...

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Bibliographic Details
Published in:Transplantation proceedings Vol. 47; no. 1; pp. 158 - 160
Main Authors: Caliskan, B, Yazici, H, Gulluoglu, M, Caliskan, Y, Turkmen, A, Sever, M.S
Format: Journal Article
Language:English
Published: United States Elsevier Inc 2015
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Summary:Abstract Chronic granulomatous disease (CGD) is a genetic disease caused by structural mutations in the enzyme NADPH oxidase that results in severe immunodeficiency. End-stage renal disease occurs in this patient population and is attributed to various factors, including infections, amyloidosis, and nephrotoxic anti-infective agents. In this report, we present our experience in transplantation for a patient with CGD complicated by isolated hepatic tuberculosis abscess. The course of the case demonstrates the absolute requirements for a multidisciplinary and compulsive approach before, during, and after transplantation. This case report also highlights the unexpectedly benign effects of immunosuppressive therapy in this patient population.
Bibliography:ObjectType-Case Study-2
SourceType-Scholarly Journals-1
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ISSN:0041-1345
1873-2623
DOI:10.1016/j.transproceed.2014.07.069