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Case report: IgG4-related renal disease co-existing with retroperitoneal fibrosis

A 51-year-old woman visited our clinic for orthopnea, chest discomfort, and facial and leg edema. Acute kidney injury and pleural effusion were diagnosed and she received hemodialysis. This is a rare case of IgG4-related disease diagnosed by renal biopsy in the patient with retroperitoneal fibrosis...

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Autores principales: Kim, Young Jin, Kim, Ga-Eon, Ma, Seong Kwon, Kim, Soo Wan, Bae, Eun Hui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7215037/
https://www.ncbi.nlm.nih.gov/pubmed/32420186
http://dx.doi.org/10.21037/tau.2020.02.06
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author Kim, Young Jin
Kim, Ga-Eon
Ma, Seong Kwon
Kim, Soo Wan
Bae, Eun Hui
author_facet Kim, Young Jin
Kim, Ga-Eon
Ma, Seong Kwon
Kim, Soo Wan
Bae, Eun Hui
author_sort Kim, Young Jin
collection PubMed
description A 51-year-old woman visited our clinic for orthopnea, chest discomfort, and facial and leg edema. Acute kidney injury and pleural effusion were diagnosed and she received hemodialysis. This is a rare case of IgG4-related disease diagnosed by renal biopsy in the patient with retroperitoneal fibrosis and severe acute kidney injury, which progressed rapidly and required hemodialysis without markedly elevated serum IgG4 level and urinary tract obstruction. Immunostaining of a kidney biopsy revealed IgG4-related renal disease and magnetic resonance imaging showed retroperitoneal fibrosis in the paraspinal and presacral areas. After 3 days of glucocorticoid treatment, renal function and bilateral pleural effusion were restored. Another 2 months of glucocorticoid treatment decreased the extent of retroperitoneal fibrosis on follow-up abdominal computed tomography. IgG4-related disease is a recently recognized fibro-inflammatory condition with a dense lymphoplasmacytic infiltration of IgG4-positive plasma cells. The kidney and retroperitoneum are the frequently associated organs in IgG4-related disease. This case shows that IgG4-related disease can involve the kidney and/or other organs and be diagnosed by kidney biopsy.
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spelling pubmed-72150372020-05-15 Case report: IgG4-related renal disease co-existing with retroperitoneal fibrosis Kim, Young Jin Kim, Ga-Eon Ma, Seong Kwon Kim, Soo Wan Bae, Eun Hui Transl Androl Urol Case Report A 51-year-old woman visited our clinic for orthopnea, chest discomfort, and facial and leg edema. Acute kidney injury and pleural effusion were diagnosed and she received hemodialysis. This is a rare case of IgG4-related disease diagnosed by renal biopsy in the patient with retroperitoneal fibrosis and severe acute kidney injury, which progressed rapidly and required hemodialysis without markedly elevated serum IgG4 level and urinary tract obstruction. Immunostaining of a kidney biopsy revealed IgG4-related renal disease and magnetic resonance imaging showed retroperitoneal fibrosis in the paraspinal and presacral areas. After 3 days of glucocorticoid treatment, renal function and bilateral pleural effusion were restored. Another 2 months of glucocorticoid treatment decreased the extent of retroperitoneal fibrosis on follow-up abdominal computed tomography. IgG4-related disease is a recently recognized fibro-inflammatory condition with a dense lymphoplasmacytic infiltration of IgG4-positive plasma cells. The kidney and retroperitoneum are the frequently associated organs in IgG4-related disease. This case shows that IgG4-related disease can involve the kidney and/or other organs and be diagnosed by kidney biopsy. AME Publishing Company 2020-04 /pmc/articles/PMC7215037/ /pubmed/32420186 http://dx.doi.org/10.21037/tau.2020.02.06 Text en 2020 Translational Andrology and Urology. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Case Report
Kim, Young Jin
Kim, Ga-Eon
Ma, Seong Kwon
Kim, Soo Wan
Bae, Eun Hui
Case report: IgG4-related renal disease co-existing with retroperitoneal fibrosis
title Case report: IgG4-related renal disease co-existing with retroperitoneal fibrosis
title_full Case report: IgG4-related renal disease co-existing with retroperitoneal fibrosis
title_fullStr Case report: IgG4-related renal disease co-existing with retroperitoneal fibrosis
title_full_unstemmed Case report: IgG4-related renal disease co-existing with retroperitoneal fibrosis
title_short Case report: IgG4-related renal disease co-existing with retroperitoneal fibrosis
title_sort case report: igg4-related renal disease co-existing with retroperitoneal fibrosis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7215037/
https://www.ncbi.nlm.nih.gov/pubmed/32420186
http://dx.doi.org/10.21037/tau.2020.02.06
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