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A Case of Fibrillary Glomerulonephritis

Fibrillary glomerulonephritis (FGN) is a very rare manifestation of glomerulonephritis characterized by the presence of deposits of randomly oriented microfibrils (10-30 nm size) in the glomeruli and visible on electron microscopy. Our patient is a 63-year-old African American male who presented wit...

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Detalles Bibliográficos
Autores principales: Venkataraj, Maamannan, Morisetti, Phani P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9490443/
https://www.ncbi.nlm.nih.gov/pubmed/36158379
http://dx.doi.org/10.7759/cureus.28250
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author Venkataraj, Maamannan
Morisetti, Phani P
author_facet Venkataraj, Maamannan
Morisetti, Phani P
author_sort Venkataraj, Maamannan
collection PubMed
description Fibrillary glomerulonephritis (FGN) is a very rare manifestation of glomerulonephritis characterized by the presence of deposits of randomly oriented microfibrils (10-30 nm size) in the glomeruli and visible on electron microscopy. Our patient is a 63-year-old African American male who presented with a past medical history of cirrhosis; he was initially suspected to have hepatorenal syndrome, but on kidney biopsy, and was diagnosed with FGN. Possible multiple myeloma was suspected due to its strong association with FGN and an elevated serum kappa-lambda ratio in the patient. This was confirmed by bone biopsy to be smoldering myeloma.
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spelling pubmed-94904432022-09-23 A Case of Fibrillary Glomerulonephritis Venkataraj, Maamannan Morisetti, Phani P Cureus Internal Medicine Fibrillary glomerulonephritis (FGN) is a very rare manifestation of glomerulonephritis characterized by the presence of deposits of randomly oriented microfibrils (10-30 nm size) in the glomeruli and visible on electron microscopy. Our patient is a 63-year-old African American male who presented with a past medical history of cirrhosis; he was initially suspected to have hepatorenal syndrome, but on kidney biopsy, and was diagnosed with FGN. Possible multiple myeloma was suspected due to its strong association with FGN and an elevated serum kappa-lambda ratio in the patient. This was confirmed by bone biopsy to be smoldering myeloma. Cureus 2022-08-22 /pmc/articles/PMC9490443/ /pubmed/36158379 http://dx.doi.org/10.7759/cureus.28250 Text en Copyright © 2022, Venkataraj et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Internal Medicine
Venkataraj, Maamannan
Morisetti, Phani P
A Case of Fibrillary Glomerulonephritis
title A Case of Fibrillary Glomerulonephritis
title_full A Case of Fibrillary Glomerulonephritis
title_fullStr A Case of Fibrillary Glomerulonephritis
title_full_unstemmed A Case of Fibrillary Glomerulonephritis
title_short A Case of Fibrillary Glomerulonephritis
title_sort case of fibrillary glomerulonephritis
topic Internal Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9490443/
https://www.ncbi.nlm.nih.gov/pubmed/36158379
http://dx.doi.org/10.7759/cureus.28250
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