Association of monoclonal gammopathy of undetermined significance and C3 glomerulopathy

Author:

Ekladious Adel12,Bhandari Ritesh3ORCID,Javaid Muhammad M.456

Affiliation:

1. Department of General Medicine and Acute Assessment Unit Canberra Hospital Canberra Australian Capital Territory Australia

2. Faculty of Health and Medical Sciences University of Western Australia Perth Western Australia Australia

3. Department of General Medicine Royal Hobart Hospital Hobart Tasmania Australia

4. Department of Renal Medicine Woodlands Health Singapore Singapore

5. School of Medicine Monash University Melbourne Victoria Australia

6. School of Medicine Deakin University Burwood Victoria Australia

Abstract

AbstractMonoclonal gammopathy of undetermined significance (MGUS) is usually an asymptomatic pre‐malignant condition caused by the proliferation of clonal plasma cells. Often considered a benign condition, it has the potential to progress to malignant plasma cell or lymphoproliferative disorders. Moreover, MGUS can rarely cause glomerular disease by activating the alternative complement pathway resulting in immunoglobulin‐negative C3‐positive glomerulonephritis called C3 glomerulopathy. Because of its rarity, the diagnosis might not be considered by the treating physicians, leading to delayed diagnosis or misdiagnosis. Untreated C3 glomerulopathy can lead to irreversible glomerular damage and end‐stage renal failure, and a high index of suspicion is essential for timely diagnosis and management. Here, we present the case of a patient with a prior diagnosis of MGUS who presented with proteinuria and microscopic haematuria and was diagnosed with C3 glomerulopathy. The patient had complete resolution of the disease after receiving treatment with a combination of dexamethasone, lenalidomide and bortezomib for the underlying MGUS.

Publisher

Wiley

Subject

Internal Medicine

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