IgG4‐related disease associated with the primary manifestation of recurrent cerebral venous thrombosis: A rare case report

Nervous system involvement in IgG4‐related systemic disease (IgG4‐RD) is rarely reported and manifests as hypertrophic pachymeningitis and hypophysitis. In this report, a 33‐year‐old woman with neurological manifestations was diagnosed with IgG4‐RD by biopsy. The patient showed improvement in sympto...

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Autores principales: Haj Mohamad Ebrahim Ketabforoush, Arsh, Bahadorinia, Mahsa, Dolatshahi, Elahe, Nozarian, Zohreh, Abbasi Khoshsirat, Nahid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9474911/
https://www.ncbi.nlm.nih.gov/pubmed/36177072
http://dx.doi.org/10.1002/ccr3.6324
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author Haj Mohamad Ebrahim Ketabforoush, Arsh
Bahadorinia, Mahsa
Dolatshahi, Elahe
Nozarian, Zohreh
Abbasi Khoshsirat, Nahid
author_facet Haj Mohamad Ebrahim Ketabforoush, Arsh
Bahadorinia, Mahsa
Dolatshahi, Elahe
Nozarian, Zohreh
Abbasi Khoshsirat, Nahid
author_sort Haj Mohamad Ebrahim Ketabforoush, Arsh
collection PubMed
description Nervous system involvement in IgG4‐related systemic disease (IgG4‐RD) is rarely reported and manifests as hypertrophic pachymeningitis and hypophysitis. In this report, a 33‐year‐old woman with neurological manifestations was diagnosed with IgG4‐RD by biopsy. The patient showed improvement in symptoms after treatment.
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spelling pubmed-94749112022-09-28 IgG4‐related disease associated with the primary manifestation of recurrent cerebral venous thrombosis: A rare case report Haj Mohamad Ebrahim Ketabforoush, Arsh Bahadorinia, Mahsa Dolatshahi, Elahe Nozarian, Zohreh Abbasi Khoshsirat, Nahid Clin Case Rep Case Report Nervous system involvement in IgG4‐related systemic disease (IgG4‐RD) is rarely reported and manifests as hypertrophic pachymeningitis and hypophysitis. In this report, a 33‐year‐old woman with neurological manifestations was diagnosed with IgG4‐RD by biopsy. The patient showed improvement in symptoms after treatment. John Wiley and Sons Inc. 2022-09-14 /pmc/articles/PMC9474911/ /pubmed/36177072 http://dx.doi.org/10.1002/ccr3.6324 Text en © 2022 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Case Report
Haj Mohamad Ebrahim Ketabforoush, Arsh
Bahadorinia, Mahsa
Dolatshahi, Elahe
Nozarian, Zohreh
Abbasi Khoshsirat, Nahid
IgG4‐related disease associated with the primary manifestation of recurrent cerebral venous thrombosis: A rare case report
title IgG4‐related disease associated with the primary manifestation of recurrent cerebral venous thrombosis: A rare case report
title_full IgG4‐related disease associated with the primary manifestation of recurrent cerebral venous thrombosis: A rare case report
title_fullStr IgG4‐related disease associated with the primary manifestation of recurrent cerebral venous thrombosis: A rare case report
title_full_unstemmed IgG4‐related disease associated with the primary manifestation of recurrent cerebral venous thrombosis: A rare case report
title_short IgG4‐related disease associated with the primary manifestation of recurrent cerebral venous thrombosis: A rare case report
title_sort igg4‐related disease associated with the primary manifestation of recurrent cerebral venous thrombosis: a rare case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9474911/
https://www.ncbi.nlm.nih.gov/pubmed/36177072
http://dx.doi.org/10.1002/ccr3.6324
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