Neurosarcoidosis: Clinical Features, Pathophysiology, and Management
Document Type
Article
Publication Date
1-1-2018
Abstract
Sarcoidosis is an immune-mediated, multisystem, inflammatory disorder of unknown etiology, which primarily affects pulmonary and lymphatic systems as well as skin. The pathologic hallmark of sarcoidosis is noncaseating epithelioid granulomas, which develop in the affected organs. Uncommonly, both central and peripheral nervous systems are affected by sarcoidosis, and patients with neurosarcoidosis present with a wide spectrum of neurologic manifestations due to the widespread nature of the underlying illness. While nervous system involvement in sarcoidosis is uncommon, in a certain number of patients, neurologic symptoms can be the initial and exclusive manifestation of sarcoidosis. Neurosarcoidosis is a great imitator of other pathologies and high clinical vigilance is required to diagnose it correctly. A discussion of the clinical features, underlying pathophysiology, and present management options for neurosarcoidosis is presented.
Publication Source (Journal or Book title)
Neuroinflammation
First Page
233
Last Page
246
Recommended Citation
Turabova, C., Reynolds, C., Minagar, A., & Davis, D. (2018). Neurosarcoidosis: Clinical Features, Pathophysiology, and Management. Neuroinflammation, 233-246. https://doi.org/10.1016/B978-0-12-811709-5.00012-0