Progressive Cranial Nerve Deficits in Granulomatosis With Polyangiitis: A Case Report.
Document Type
Article
Publication Date
6-19-2025
Publication Title
Cureus
Abstract
Granulomatosis with polyangiitis (GPA) is a rare systemic vasculitis that can involve multiple organ systems, including the nervous system. Central nervous system (CNS) involvement, especially in the form of cranial nerve neuropathy, is uncommon and may present with significant diagnostic challenges. This case report details the presentation, diagnostic workup, and management of a 60-year-old female who initially developed unilateral cranial nerve deficits, which progressed to bilateral involvement over an 11-day hospital course. The purpose of this case report is to highlight the importance of including GPA in the differential diagnosis in the setting of progressive cranial neuropathy, and to emphasize the need for a multidisciplinary approach for timely diagnosis and utilization of immunosuppressive treatment to minimize the chronic effects of the disease.
Volume
17
Issue
6
First Page
e86364
Recommended Citation
Waggoner R, Bitar I, Pavuloori M, Yako A, Kizy N. Progressive cranial nerve deficits in granulomatosis with polyangiitis: A case report. Cureus. 2025 Jun 19;17(6):e86364. doi: 10.7759/cureus.86364. PMID: 40688874
DOI
10.7759/cureus.86364
ISSN
2168-8184
PubMed ID
40688874