Light-Chain Deposition Disease Presenting with Spontaneous Splenic Rupture.

Eur J Case Rep Intern Med

Serviço de Medicina 1, ULSAM, Viana do Castelo, Portugal.

Published: December 2018

Unlabelled: Light-chain deposition disease is a rare paraproteinaemia characterized by deposition of monoclonal light-chain immunoglobulins with a non-amyloid structure, most frequently affecting the kidney. The authors present the case of a 58-year-old man admitted due to haemorrhagic shock caused by spontaneous splenic rupture. Investigation showed coagulopathy, homogeneous hepatomegaly with elevated cholestasis enzymes but normal bilirubinaemia, and a nephrotic syndrome with monoclonal kappa light chains. Liver and bone marrow biopsies revealed light-chain deposition disease. Splenic rupture as the presentation of a paraproteinaemia is rare. The diagnosis of light-chain deposition disease should be considered in case of a monoclonal plasma cell disorder with Congo-red negative deposits on histology.

Learning Points: Spontaneous splenic rupture is a rare presentation of a paraproteinaemia.Light-chain deposition disease is a rare disease with non-fibrillar deposition of monoclonal light-chain immunoglobulins most frequently affecting the kidney.Light-chain deposition disease should be suspected in case of a monoclonal plasma cell disorder with Congo-red negative deposits on histology.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6346975PMC
http://dx.doi.org/10.12890/2018_0001010DOI Listing

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