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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AME Publishing Company
2020
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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. |
format | Online Article Text |
id | pubmed-7215037 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | AME Publishing Company |
record_format | MEDLINE/PubMed |
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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