| Literature DB >> 34517153 |
Christelle Nilles1, Guillaume Poillon2, Lydia Deschamps3, Mary Daval4, Ibrahima Mariam Diallo5, Romain Deschamps1, Marine Boudot de la Motte6.
Abstract
IgG4-related disease (IgG4-RD) is a multisystem fibroinflammatory condition; this can be a challenging diagnosis that requires clinico-pathologic correlation. We report a young woman, presenting with cranial nerve palsy. The work-up revealed pachymeningitis, cerebral venous thrombosis (CVT), and a destructive lesion in the mastoid. We diagnosed IgG4-RD through mastoidectomy. Thus, a biopsy of asymptomatic, infrequently affected organs, like the mastoid, can meet all histopathological criteria. In neuro-meningeal presentations, CVT may be secondary to the local inflammatory environment of pachymeningitis. Since our patient had a deep vein thrombosis one year prior, we discuss a possible higher risk of thrombosis in IgG4-RD patients.Entities:
Keywords: Cerebral venous thrombosis; Classification criteria; Clinico-pathologic confirmation; IgG4-related disease; Inflammatory pseudotumor; Skull base
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Year: 2021 PMID: 34517153 DOI: 10.1016/j.jneuroim.2021.577717
Source DB: PubMed Journal: J Neuroimmunol ISSN: 0165-5728 Impact factor: 3.478