ArticleRheumatology international2026
Sarcoidosis-like reaction associated with tocilizumab in a patient with giant cell arteritis: a case based review.
Article in Rheumatology international, 2026. 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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Abstract
We report a 71-year-old man with confirmed giant cell arteritis (GCA) who underwent temporal artery biopsy. Following 2.5 years of combination therapy with tocilizumab (TCZ) (162 mg/w) and glucocorticoids (tapered over 2.5 years to prednisolone 1 mg/day), erythematous facial papules and red eye developed. Skin biopsy revealed multiple non-caseating epithelioid granulomas containing multinucleated giant cells, without evidence of infection. Serum angiotensin-converting enzyme levels and soluble interleukin-2 receptor levels were within normal limits, and imaging showed no systemic sarcoidosis involvement. TCZ-induced sarcoidosis-like reaction was suspected. TCZ was discontinued 3 months after the onset of the lesions. Considering the risk of GCA recurrence, PSL was increased to 2 mg/day. The erythematous facial papules and red eye showed improvement 5 months after the onset of the lesions. There was no GCA recurrence. Biologic agents including TCZ are cornerstones in autoimmune disease management but may paradoxically induce immune-mediated reactions, including sarcoidosis-like reactions due to immune dysregulation. A literature search identified 6 previously published cases of TCZ-associated sarcoidosis-like reactions. Among these, ocular involvement in the form of scleritis was observed only in the present case. We should remain vigilant for sarcoidosis-like reaction during TCZ therapy and consider individualized monitoring and treatment adjustment.
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