ArticleCureus2025
Osseous Sarcoidosis of the Clivus Causing Cranial Nerve VI Palsy: A Case Report.
Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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5 authors.
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Abstract
Sarcoidosis is an inflammatory condition characterized by the presence of noncaseating, or nonnecrotizing, granulomas in one or more organ systems. It has a wide range of clinical presentations and often mimics other conditions, making it difficult to diagnose. Osseous sarcoidosis of the skull base is extremely rare and has not previously been reported in a young adult patient. A 20-year-old man with a prior diagnosis of chronic recurrent multifocal osteomyelitis and pulmonary nodules of unknown etiology presented with six weeks of intractable headache and eye pain, followed by acute-onset complete right-sided sixth cranial nerve palsy. Imaging revealed a lesion of his clivus, extending into the cavernous sinus, along with inflammation of his paranasal sinuses. Extensive workup was negative for infection. Histopathological analysis of a biopsy of the lesion showed chronic inflammation with nonnecrotizing granulomas without evidence of infection or vasculitis, supporting a diagnosis of sarcoidosis. He was treated with prednisone, adalimumab, and adjunctive methotrexate, and had resolution of his symptoms after six months. Osseous involvement in sarcoidosis is uncommon, particularly in the pediatric and young adult populations. Although rare, sarcoidosis should be included in the differential diagnosis for patients with sterile, inflammatory bone lesions. Careful evaluation for additional clinical features of sarcoidosis and thorough histopathological evaluation of the bone biopsy for evidence of granulomatous inflammation, as well as exclusion of alternative etiologies of granulomatous disease, help distinguish these conditions.
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