Tumor necrosis factor inhibitors for pediatric patients with SAPHO syndrome associated with acne conglobata
Abstract Synovitis, acne, pustulosis, hyperostosis, and osteitis (SAPHO) syndrome is a rare chronic inflammatory disease with osteoarticular and cutaneous involvements as its main manifestations. Acne conglobata as a severe acne form may affect adolescent patients. Tumor necrosis factor inhibitors a...
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2022-10-01T00:00:00Z.
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| LEADER | 00000 am a22000003u 4500 | ||
|---|---|---|---|
| 001 | doaj_d0c09dad6a504e73b47fe8e74d4dd57d | ||
| 042 | |a dc | ||
| 100 | 1 | 0 | |a Shengyan Liu |e author |
| 700 | 1 | 0 | |a Xia Wu |e author |
| 700 | 1 | 0 | |a Yihan Cao |e author |
| 700 | 1 | 0 | |a Zhaohui Li |e author |
| 700 | 1 | 0 | |a Yuchen Liu |e author |
| 700 | 1 | 0 | |a Mingwei Ma |e author |
| 700 | 1 | 0 | |a Chen Li |e author |
| 245 | 0 | 0 | |a Tumor necrosis factor inhibitors for pediatric patients with SAPHO syndrome associated with acne conglobata |
| 260 | |b BMC, |c 2022-10-01T00:00:00Z. | ||
| 500 | |a 10.1186/s12969-022-00749-9 | ||
| 500 | |a 1546-0096 | ||
| 520 | |a Abstract Synovitis, acne, pustulosis, hyperostosis, and osteitis (SAPHO) syndrome is a rare chronic inflammatory disease with osteoarticular and cutaneous involvements as its main manifestations. Acne conglobata as a severe acne form may affect adolescent patients. Tumor necrosis factor inhibitors are usually used as a second-line therapy for refractory SAPHO syndrome and has been reported to treat acne conglobata successfully. We herein report three cases of adolescent patients with SAPHO syndrome associated with acne conglobata who were successfully treated with TNFi therapy. | ||
| 546 | |a EN | ||
| 690 | |a Acne conglobata | ||
| 690 | |a Tumor necrosis factor inhibitor | ||
| 690 | |a SAPHO syndrome | ||
| 690 | |a Pediatrics | ||
| 690 | |a RJ1-570 | ||
| 690 | |a Diseases of the musculoskeletal system | ||
| 690 | |a RC925-935 | ||
| 655 | 7 | |a article |2 local | |
| 786 | 0 | |n Pediatric Rheumatology Online Journal, Vol 20, Iss 1, Pp 1-3 (2022) | |
| 787 | 0 | |n https://doi.org/10.1186/s12969-022-00749-9 | |
| 787 | 0 | |n https://doaj.org/toc/1546-0096 | |
| 856 | 4 | 1 | |u https://doaj.org/article/d0c09dad6a504e73b47fe8e74d4dd57d |z Connect to this object online. |