SAPHO syndrome complicated by IgG4-related ophthalmic disease: a case report and literature review

IntroductionSynovitis, acne, pustulosis, hyperostosis, and osteitis (SAPHO) syndrome is an extremely rare condition with nonspecific clinical signs and symptoms.Case descriptionHere, we present the case of a 54-year-old Chinese woman with an 8-year history of recurrent furuncles and a 6-year history...

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Bibliographic Details
Main Authors: Chenxiao Liu, Tingting Chen, Yanyan Wang, Qi Wang, Hao Hu, Huanhuan Chen
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-04-01
Series:Frontiers in Immunology
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Online Access:https://www.frontiersin.org/articles/10.3389/fimmu.2025.1563542/full
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