Affiliation:
1. Department of Rheumatology Dongfang Hospital Beijing University of Chinese Medicine Beijing China
2. Department of Rheumatology Fangshan Hospital Beijing University of Chinese Medicine Beijing China
Abstract
AbstractSynovitis, acne, pustulosis, hyperostosis, and osteitis (SAPHO) syndrome is a rare chronic inflammatory disease. The main clinical manifestation of SAPHO syndrome is an osteoarthropathy with cutaneous involvement. Relapsing polychondritis (RP) characterized by chronic inflammation and cartilage degeneration is a rare systematic autoimmune disease. Here we report a RP case in a SAPHO syndrome patient, in which auricularitis happened 10 years after the diagnosed as SAPHO syndrome. Tofacitinib treatment can alleviate the symptoms.
Funder
National Natural Science Foundation of China
Cited by
3 articles.
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