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SAPHO syndrome with Takayasu arteritis successfully treated with tofacitinib.

Chen RuTangliang QianXiaoping LiuChaoxin WangWeizhong LiXiu-Juan HouXiujuan Hou
Published in: International journal of rheumatic diseases (2023)
SAPHO syndrome is an autoinflammatory disease with a variety of clinical manifestations, which may be accompanied by other systemic inflammatory diseases in addition to the typical manifestations of common synovitis, acne, pustulosis, hyperostosis, and osteitis. Here, we report the first case of SAPHO syndrome combined with Takayasu arteritis.
Keyphrases
  • case report
  • oxidative stress