SAPHO syndrome with Takayasu arteritis successfully treated with tofacitinib
Ru Chen, Tangliang Qian, Xiaoping Liu, Chaoxin Wang, Weizhong Li, Xiujuan Hou, Chen Li
Abstract
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.
Topics & Concepts
SAPHO syndromeMedicinePustulosisDermatologySynovitisOsteitisHyperostosisTofacitinibAcneTakayasu's arteritisDiseaseInternal medicineArthritisRheumatoid arthritisSurgeryVasculitisOsteomyelitisOsteomyelitis and Bone Disorders ResearchInflammasome and immune disordersOral Health Pathology and Treatment