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IgG4 ‐related disease associated with the primary manifestation of recurrent cerebral venous thrombosis: A rare case report
Author(s) -
Haj Mohamad Ebrahim Ketabforoush Arsh,
Bahadorinia Mahsa,
Dolatshahi Elahe,
Nozarian Zohreh,
Abbasi Khoshsirat Nahid
Publication year - 2022
Publication title -
clinical case reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.21
H-Index - 9
ISSN - 2050-0904
DOI - 10.1002/ccr3.6324
Subject(s) - medicine , venous thrombosis , rare disease , hypophysitis , disease , igg4 related disease , thrombosis , radiology , surgery , pathology , hormone , pituitary gland
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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