Monoclonal Gammopathy of Renal Significance (MGRS) – Case Series from a Tertiary Center in Kerala

Author:

Padmanabhan Priya,P Jayameena1,Mampilly Neena2,Francis Shinto3,Sherif Ajmal4,George Sunil1,Mathew Thomas1

Affiliation:

1. Department of Nephrology, Baby Memorial Hospital, Kozhikode, Kerala, India

2. Department of Pathology, Baby Memorial Hospital, Kozhikode, Kerala, India

3. Department of Clinical Hematology and Hematooncology, Baby Memorial Hospital, Kozhikode, Kerala, India

4. Senior Consultant Medical Oncologist, American Oncology Institute, Kozhikode, Kerala, India

Abstract

Monoclonal gammopathy of renal significance (MGRS) has gained importance because identifying the monoclonal deposit and addressing it, rather than treating renal dysfunction as the primary pathology, has salvaged the patients from progressing into end-stage renal disease. Since it affects elderly population, there could be a propensity to misdiagnose them with cardiorenal syndrome. We present four patients of MGRS diagnosed from our center. They presented with proteinuria or unexplained renal dysfunction. Three of the patients were diagnosed to have amyloidosis, of which two had lambda-type and one had kappa amyloidosis. The fourth patient had fibrillary glomerulonephritis with kappa restriction, further evaluation of which led to diagnosis of chronic lymphocytic leukemia. Absence of “M” band in protein electrophoresis and a normal bone marrow study should not stop physicians from further evaluation. Quantitative serum immunofixation electrophoresis and electron microscopic examination of renal biopsy have become a comprehensive diagnostic tool in such patients.

Publisher

Scientific Scholar

Reference9 articles.

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