| Literature DB >> 32595131 |
Rebaika Chopra1, Rosalba Santana de Roberts2, Ibrahim Batal3, Sachin Batra1, Belinda Jim4.
Abstract
Kidney tubular disorders due to monoclonal immunoglobulin light chains are common manifestations of B-cell neoplasm. Cast nephropathy (CN) is the most frequent type of these disorders and may present with acute kidney injury (AKI) due to the presence of excess light chains in the distal tubules. Light chain proximal tubulopathy (LCPT) is an uncommon form of renal disease and may present as Fanconi syndrome due to proximal tubular cell damage by intracellular deposition of light chains. The concomitant disorder of both CN and LCPT is rare given the inherent differences in the biochemical properties of the immunoglobulin light chains of each disorder. We report a 64-year-old man who presented with AKI and Fanconi syndrome who was discovered to have both CN and LCPT due to the underlying disorder of monoclonal gammopathy of renal significance and who has responded favourably with conventional chemotherapy. We also review the existing literature on this interesting subject. © BMJ Publishing Group Limited 2020. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: acute renal failure; chemotherapy; haematology (incl blood transfusion); proteinurea; renal system
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Year: 2020 PMID: 32595131 PMCID: PMC7322277 DOI: 10.1136/bcr-2020-234361
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X