SAPHO syndrome with Takayasu arteritis successfully treated with tofacitinib

被引：7

作者：

Ru, Chen ^{[1
,2
]}

Qian, Tangliang ^{[1
,2
]}

Liu, Xiaoping ^{[2
]}

Wang, Chaoxin ^{[2
]}

Li, Weizhong ^{[3
]}

Hou, Xiujuan ^{[2
]}

Li, Chen ^{[3
]}

机构：

[1] Beijing Univ Chinese Med, Beijing, Peoples R China

[2] Beijing Univ Chinese Med, Dongfang Hosp, Dept Rheumatol, Beijing, Peoples R China

[3] Beijing Univ Chinese Med, Fangshan Hosp, Dept Rheumatol, Beijing, Peoples R China

来源：

INTERNATIONAL JOURNAL OF RHEUMATIC DISEASES | 2023年 / 26卷 / 07期

基金：

中国国家自然科学基金;

关键词：

SAPHO syndrome; Takayasu arteritis; tofacitinib;

D O I：

10.1111/1756-185X.14628

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

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.

引用

页码：1381 / 1383

页数：3

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