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

Autor: Haj Mohamad Ebrahim Ketabforoush A; Cellular and Molecular Research Center Iran University of Medical Sciences Tehran Iran., Bahadorinia M; Student Research Committee Alborz University of Medical Sciences Karaj Iran., Dolatshahi E; Department of Rheumatology Clinical Research Development Unit (CRDU) of Shahid Rajaei Hospital Alborz University of Medical Sciences Karaj Iran., Nozarian Z; Department of Pathology Farabi Eye Hospital Tehran University of Medical Sciences Tehran Iran., Abbasi Khoshsirat N; Department of Neurology Clinical Research Development Unit (CRDU) of Shahid Rajaei Hospital Alborz University of Medical Sciences Karaj Iran.
Jazyk: angličtina
Zdroj: Clinical case reports [Clin Case Rep] 2022 Sep 14; Vol. 10 (9), pp. e6324. Date of Electronic Publication: 2022 Sep 14 (Print Publication: 2022).
DOI: 10.1002/ccr3.6324
Abstrakt: 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.
Competing Interests: All authors declare that there is no conflict of interest with respect to the research, authorship, and/or publication of this article.
(© 2022 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd.)
Databáze: MEDLINE
Externí odkaz:
Nepřihlášeným uživatelům se plný text nezobrazuje