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IgG4-Related Kidney Disease Associated With End-Stage Kidney Disease, Renal Pseudotumor, and Renal Vein Thrombosis

IgG4 related disease (IgG4-RD) is a systemic autoimmune disease characterized by tissue invasion with IgG4-producing plasma cells, resulting in tissue dysfunction. IgG4-RD can affect the kidney in various forms, including renal mass, tubulointerstitial disease, and glomerulonephritis. IgG4-RD can mi...

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Autores principales: Tawhari, Mohammed, Al Oudah, Nourah, Al Zahrani, Yousof, Radwi, Mansoor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8906446/
https://www.ncbi.nlm.nih.gov/pubmed/35281583
http://dx.doi.org/10.7759/cureus.22837
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author Tawhari, Mohammed
Al Oudah, Nourah
Al Zahrani, Yousof
Radwi, Mansoor
author_facet Tawhari, Mohammed
Al Oudah, Nourah
Al Zahrani, Yousof
Radwi, Mansoor
author_sort Tawhari, Mohammed
collection PubMed
description IgG4 related disease (IgG4-RD) is a systemic autoimmune disease characterized by tissue invasion with IgG4-producing plasma cells, resulting in tissue dysfunction. IgG4-RD can affect the kidney in various forms, including renal mass, tubulointerstitial disease, and glomerulonephritis. IgG4-RD can mimic other autoimmune diseases and neoplasms, and as such, maintaining a high index of suspicion is the key to timely diagnosis and treatment. In this paper, we present a case of IgG4-RD that presented with pseudotumor and severe renal dysfunction that progressed to end-stage kidney disease (ESKD), associated with a rare finding of renal vein thrombosis (RVT).
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spelling pubmed-89064462022-03-10 IgG4-Related Kidney Disease Associated With End-Stage Kidney Disease, Renal Pseudotumor, and Renal Vein Thrombosis Tawhari, Mohammed Al Oudah, Nourah Al Zahrani, Yousof Radwi, Mansoor Cureus Internal Medicine IgG4 related disease (IgG4-RD) is a systemic autoimmune disease characterized by tissue invasion with IgG4-producing plasma cells, resulting in tissue dysfunction. IgG4-RD can affect the kidney in various forms, including renal mass, tubulointerstitial disease, and glomerulonephritis. IgG4-RD can mimic other autoimmune diseases and neoplasms, and as such, maintaining a high index of suspicion is the key to timely diagnosis and treatment. In this paper, we present a case of IgG4-RD that presented with pseudotumor and severe renal dysfunction that progressed to end-stage kidney disease (ESKD), associated with a rare finding of renal vein thrombosis (RVT). Cureus 2022-03-04 /pmc/articles/PMC8906446/ /pubmed/35281583 http://dx.doi.org/10.7759/cureus.22837 Text en Copyright © 2022, Tawhari 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
Tawhari, Mohammed
Al Oudah, Nourah
Al Zahrani, Yousof
Radwi, Mansoor
IgG4-Related Kidney Disease Associated With End-Stage Kidney Disease, Renal Pseudotumor, and Renal Vein Thrombosis
title IgG4-Related Kidney Disease Associated With End-Stage Kidney Disease, Renal Pseudotumor, and Renal Vein Thrombosis
title_full IgG4-Related Kidney Disease Associated With End-Stage Kidney Disease, Renal Pseudotumor, and Renal Vein Thrombosis
title_fullStr IgG4-Related Kidney Disease Associated With End-Stage Kidney Disease, Renal Pseudotumor, and Renal Vein Thrombosis
title_full_unstemmed IgG4-Related Kidney Disease Associated With End-Stage Kidney Disease, Renal Pseudotumor, and Renal Vein Thrombosis
title_short IgG4-Related Kidney Disease Associated With End-Stage Kidney Disease, Renal Pseudotumor, and Renal Vein Thrombosis
title_sort igg4-related kidney disease associated with end-stage kidney disease, renal pseudotumor, and renal vein thrombosis
topic Internal Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8906446/
https://www.ncbi.nlm.nih.gov/pubmed/35281583
http://dx.doi.org/10.7759/cureus.22837
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