Neurosarcoidosis
https://doi.org/10.30629/0023-2149-2025-103-12-865-872
Abstract
Neurosarcoidosis is a rare manifestation of systemic sarcoidosis characterized by involvement of both the central and peripheral nervous systems. The clinical presentation is highly variable and depends on the localization of granulomatous inflammation, which complicates the diagnostic process. This article reviews current understanding of the pathogenesis, clinical phenotypes, and differential diagnosis of neurosarcoidosis. It also describes methods of neuroimaging, laboratory diagnostics, and histological verification of the disease. Special attention is given to therapeutic strategies, including glucocorticoid and immunosuppressive therapy. Prognostic considerations and potential directions for future research are discussed.
About the Authors
S. A. TerpigorevRussian Federation
Stanislav A. Terpigorev — Doctor of Medical Sciences, Head of the Department of Internal Medicine
Moscow
R. R. Bogdanov
Russian Federation
Rinat R. Bogdanov — Candidate of Medical Sciences, Associate Professor, Head of the Department of Neurology
Moscow
A. V. Dimertsev
Russian Federation
Alexey V. Dimertsev — Candidate of Medical Sciences, Neurosurgeon, Department of Neurosurgery
Moscow
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Review
For citations:
Terpigorev S.A., Bogdanov R.R., Dimertsev A.V. Neurosarcoidosis. Clinical Medicine (Russian Journal). 2025;103(12):865-872. (In Russ.) https://doi.org/10.30629/0023-2149-2025-103-12-865-872
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