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Benign Intracranial Hypertension: A Rare Manifestation of Neurosarcoidosis.

Authors :
Dubey P
Nirhale S
Rohatgi S
Khandait P
Source :
Cureus [Cureus] 2023 Aug 12; Vol. 15 (8), pp. e43363. Date of Electronic Publication: 2023 Aug 12 (Print Publication: 2023).
Publication Year :
2023

Abstract

Sarcoidosis is an immune-mediated disease that can involve multiple systems. Sarcoidosis of the nervous system or neurosarcoidosis may present as cranial mononeuropathy, hypothalamic involvement, aseptic meningitis, granulomatous inflammation in the brain parenchyma or spinal cord, peripheral neuropathy, and, in rare cases, as myopathy and benign intracranial hypertension. The most common cranial nerve involvement is the facial nerve, which can present as unilateral or bilateral facial nerve palsy, often with recurrent episodes. Involvement of other cranial nerves such as the second and eighth cranial nerves has also been reported. Granulomatous inflammation in the spinal cord presents as myelopathy or radiculopathy. Peripheral neuropathy can manifest as mononeuropathy, mononeuritis multiplex, or generalized sensory-motor neuropathy. Carpal tunnel syndrome is more common in patients with sarcoidosis compared to the general population. Here, we describe the case of a 40-year-old female who presented with heaviness of the head and blurred vision, with a prior history of left-sided Bell's palsy. Bilateral papilledema was observed during the fundus examination. MRI of the brain revealed signs suggestive of benign intracranial hypertension. The cerebrospinal fluid (CSF) opening pressure was measured at 40 cmH2O. Biopsy of bilateral hilar lymphadenopathy indicated granulomatous inflammation consistent with sarcoidosis. The patient was started on steroids and acetazolamide, and she had a dramatic improvement in symptoms.<br />Competing Interests: The authors have declared that no competing interests exist.<br /> (Copyright © 2023, Dubey et al.)

Details

Language :
English
ISSN :
2168-8184
Volume :
15
Issue :
8
Database :
MEDLINE
Journal :
Cureus
Publication Type :
Report
Accession number :
37701004
Full Text :
https://doi.org/10.7759/cureus.43363