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IgG4 Related Disease associated with the primary manifestation of recurrent Cerebral Venous Thrombosis: a rare case report
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  • Arsh Haj Mohamad Ebrahim Ketabforoush,
  • Mahsa Bahadorinia,
  • Elahe Dolatshahi,
  • Zohreh Nozarian,
  • Nahid Abbasi Khoshsirat
Arsh Haj Mohamad Ebrahim Ketabforoush
Iran University of Medical Sciences

Corresponding Author:[email protected]

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Mahsa Bahadorinia
Alborz University of Medical Sciences
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Elahe Dolatshahi
Alborz University of Medical Sciences
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Zohreh Nozarian
Tehran University of Medical Sciences
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Nahid Abbasi Khoshsirat
Alborz University of Medical Sciences
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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 the treatment.

Peer review status:ACCEPTED

16 Jul 2022Submitted to Clinical Case Reports
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19 Jul 2022Submission Checks Completed
19 Jul 2022Assigned to Editor
23 Jul 2022Reviewer(s) Assigned
02 Aug 2022Review(s) Completed, Editorial Evaluation Pending
02 Aug 2022Editorial Decision: Revise Minor
23 Aug 20221st Revision Received
26 Aug 2022Submission Checks Completed
26 Aug 2022Assigned to Editor
26 Aug 2022Review(s) Completed, Editorial Evaluation Pending
29 Aug 2022Editorial Decision: Accept