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.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom