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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:arsh.ketabforoush@yahoo.com

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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.
16 Jul 2022Submitted to Clinical Case Reports
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