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

Abstract 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...

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Main Authors: Arsh Haj Mohamad Ebrahim Ketabforoush, Mahsa Bahadorinia, Elahe Dolatshahi, Zohreh Nozarian, Nahid Abbasi Khoshsirat
Format: Article
Language:English
Published: Wiley 2022-09-01
Series:Clinical Case Reports
Subjects:
Online Access:https://doi.org/10.1002/ccr3.6324
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author Arsh Haj Mohamad Ebrahim Ketabforoush
Mahsa Bahadorinia
Elahe Dolatshahi
Zohreh Nozarian
Nahid Abbasi Khoshsirat
author_facet Arsh Haj Mohamad Ebrahim Ketabforoush
Mahsa Bahadorinia
Elahe Dolatshahi
Zohreh Nozarian
Nahid Abbasi Khoshsirat
author_sort Arsh Haj Mohamad Ebrahim Ketabforoush
collection DOAJ
description Abstract 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 doaj.art-8209974d48d54401a841b4c84dceb8c42022-12-22T04:27:14ZengWileyClinical Case Reports2050-09042022-09-01109n/an/a10.1002/ccr3.6324IgG4‐related disease associated with the primary manifestation of recurrent cerebral venous thrombosis: A rare case reportArsh Haj Mohamad Ebrahim Ketabforoush0Mahsa Bahadorinia1Elahe Dolatshahi2Zohreh Nozarian3Nahid Abbasi Khoshsirat4Cellular and Molecular Research Center Iran University of Medical Sciences Tehran IranStudent Research Committee Alborz University of Medical Sciences Karaj IranDepartment of Rheumatology Clinical Research Development Unit (CRDU) of Shahid Rajaei Hospital Alborz University of Medical Sciences Karaj IranDepartment of Pathology Farabi Eye Hospital Tehran University of Medical Sciences Tehran IranDepartment of Neurology Clinical Research Development Unit (CRDU) of Shahid Rajaei Hospital Alborz University of Medical Sciences Karaj IranAbstract 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.https://doi.org/10.1002/ccr3.6324cerebral venous thrombosisIgG4‐related diseasepachymeningitis
spellingShingle Arsh Haj Mohamad Ebrahim Ketabforoush
Mahsa Bahadorinia
Elahe Dolatshahi
Zohreh Nozarian
Nahid Abbasi Khoshsirat
IgG4‐related disease associated with the primary manifestation of recurrent cerebral venous thrombosis: A rare case report
Clinical Case Reports
cerebral venous thrombosis
IgG4‐related disease
pachymeningitis
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 cerebral venous thrombosis
IgG4‐related disease
pachymeningitis
url https://doi.org/10.1002/ccr3.6324
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