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IgG4-Related Disease coexisting with Behçet’s Disease

We describe a case of Immunoglobulin G4-related disease (IgG4-RD) coexisting with Behçet’s disease. A 49-year-old man, with a diagnosis of Behçet’s Disease for 15 years who was found to have an acute kidney injury. His investigations revealed an elevated IgG4 level and the abdominal computerized tom...

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Autores principales: Alanazi, Mohammed B., Asiri, Yahya O., Al-Homood, Ibrahim A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Mediterranean Journal of Rheumatology (MJR) 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7241657/
https://www.ncbi.nlm.nih.gov/pubmed/32467875
http://dx.doi.org/10.31138/mjr.30.4.228
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author Alanazi, Mohammed B.
Asiri, Yahya O.
Al-Homood, Ibrahim A.
author_facet Alanazi, Mohammed B.
Asiri, Yahya O.
Al-Homood, Ibrahim A.
author_sort Alanazi, Mohammed B.
collection PubMed
description We describe a case of Immunoglobulin G4-related disease (IgG4-RD) coexisting with Behçet’s disease. A 49-year-old man, with a diagnosis of Behçet’s Disease for 15 years who was found to have an acute kidney injury. His investigations revealed an elevated IgG4 level and the abdominal computerized tomography showed a retroperitoneal mass, which was diagnosed to be IgG4-RD based on histology. The patient showed symptomatic and radiological improvement after starting high dose steroid for 1 month followed by a maintenance dose. Our case report suggested that the two diseases arose separately.
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spelling pubmed-72416572020-05-27 IgG4-Related Disease coexisting with Behçet’s Disease Alanazi, Mohammed B. Asiri, Yahya O. Al-Homood, Ibrahim A. Mediterr J Rheumatol Case Report We describe a case of Immunoglobulin G4-related disease (IgG4-RD) coexisting with Behçet’s disease. A 49-year-old man, with a diagnosis of Behçet’s Disease for 15 years who was found to have an acute kidney injury. His investigations revealed an elevated IgG4 level and the abdominal computerized tomography showed a retroperitoneal mass, which was diagnosed to be IgG4-RD based on histology. The patient showed symptomatic and radiological improvement after starting high dose steroid for 1 month followed by a maintenance dose. Our case report suggested that the two diseases arose separately. The Mediterranean Journal of Rheumatology (MJR) 2019-12-31 /pmc/articles/PMC7241657/ /pubmed/32467875 http://dx.doi.org/10.31138/mjr.30.4.228 Text en © 2019 The Mediterranean Journal of Rheumatology (MJR) http://creativecommons.org/licenses/by/4.0/ This work is licensed under and Creative Commons Attribution-NonCommercial 4.0 International License.
spellingShingle Case Report
Alanazi, Mohammed B.
Asiri, Yahya O.
Al-Homood, Ibrahim A.
IgG4-Related Disease coexisting with Behçet’s Disease
title IgG4-Related Disease coexisting with Behçet’s Disease
title_full IgG4-Related Disease coexisting with Behçet’s Disease
title_fullStr IgG4-Related Disease coexisting with Behçet’s Disease
title_full_unstemmed IgG4-Related Disease coexisting with Behçet’s Disease
title_short IgG4-Related Disease coexisting with Behçet’s Disease
title_sort igg4-related disease coexisting with behçet’s disease
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7241657/
https://www.ncbi.nlm.nih.gov/pubmed/32467875
http://dx.doi.org/10.31138/mjr.30.4.228
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