Zobrazeno 1 - 10
of 1 828
pro vyhledávání: '"SAPHO syndrome"'
Autor:
Katerina Bouchalova, Zuzana Pytelova
Publikováno v:
Biomedical Papers, Vol 168, Iss 3, Pp 191-199 (2024)
Chronic recurrent multifocal osteomyelitis (CRMO), also called chronic nonbacterial osteomyelitis (CNO) or nonbacterial osteomyelitis (NBO), is a rare autoinflammatory bone disease of unknown etiology. However, the number of patients properly diagnos
Externí odkaz:
https://doaj.org/article/0ec27dd4ae9a49a68ea182810ef99565
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
SAPHO syndrome is a complex inflammatory disorder affecting the skin and bones, characterized by osteomyelitis, acne, and pustulosis. Cytokines play a pivotal role in the pathogenesis of SAPHO syndrome, especially in inflammatory responses and immune
Externí odkaz:
https://doaj.org/article/3780ab8091e144b68636fdffd8167a7e
Publikováno v:
Clinical, Cosmetic and Investigational Dermatology, Vol Volume 17, Pp 529-537 (2024)
Jianqiu Yang,1,2 Chunyu Yuan,1 Shengru Zhou,1 Zhicheng Teng,2 Min Li1 1Department of Dermatology, Dushu Lake Hospital Affiliated to Soochow University (Medical Center of Soochow University), Suzhou, People’s Republic of China; 2Suzhou Medical Colle
Externí odkaz:
https://doaj.org/article/bdc8737cd0be4a398424e66537e3f39a
Publikováno v:
Clinical, Cosmetic and Investigational Dermatology, Vol Volume 17, Pp 547-552 (2024)
Danyang Fan, Fuqiu Li, Zhe Liu, Zhanhan Tang, Sha Lv Department of Dermatology, The Second Hospital of Jilin University, Changchun, Jilin, 130000, People’s Republic of ChinaCorrespondence: Sha Lv, Department of Dermatology, The second hospital of J
Externí odkaz:
https://doaj.org/article/d88eefa7121c4c0a887ed8c6214cbafa
Publikováno v:
Journal of Medical Case Reports, Vol 18, Iss 1, Pp 1-5 (2024)
Abstract Introduction The synovitis, acne, pustulosis, hyperostosis, and osteitis (SAPHO) syndrome is a rare condition. Its treatment remains a challenge for clinicians, and often yields mixed results. Case We report the case of a 51-year-old Caucasi
Externí odkaz:
https://doaj.org/article/6fd3f2f782354eada3a0f1abce1495de
Publikováno v:
International Medical Case Reports Journal, Vol Volume 16, Pp 591-598 (2023)
Yanfeng Zhang,1 Yujia Luo,1 Yachao Ruan,2 Xiang Qian,3 Zhiying Feng1 1Department of Pain Medicine, The First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, Zhejiang, 310003, People’s Republic of China; 2Department of Radiol
Externí odkaz:
https://doaj.org/article/77f8941c847e438e8d240f6b03b248e2
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-7 (2023)
Abstract Introduction SAPHO syndrome is a group of special syndromes characterized by synovitis, acne, pustulosis, hyperostosis and osteitis. Skin lesions and joint damage are the main clinical manifestations. Among them, females mostly present with
Externí odkaz:
https://doaj.org/article/d52bad4b6666481f9ba45104c9750006
Autor:
Akira Kakiuchi, MD, Yayoi Yamamoto, MD, PhD, Akira Kanbe, MD, Daichi Kojima, MD, Ayako Hino, MD, PhD, Ayumi Horikawa, MD, PhD, Tsunehiro Doiuchi, MD, Hiroaki Kurihara, MD, PhD
Publikováno v:
Radiology Case Reports, Vol 18, Iss 10, Pp 3612-3614 (2023)
SAPHO (synovitis, acne, pustulosis, hyperostosis, and osteitis) syndrome is a rare, chronic autoinflammatory disorder that can present with a constellation of cutaneous and osteoarticular symptoms. Osteodestructive lesions are not pathognomonic, wher
Externí odkaz:
https://doaj.org/article/37cf6e52f4e94e788fdef2a2b24d89ba
Publikováno v:
Clinical, Cosmetic and Investigational Dermatology, Vol Volume 16, Pp 1089-1094 (2023)
Ruoyi Wang,1,2,* Yingzi Li,1,2,* Yuyue Liu,3 Xiujuan Hou,1,2,* Chen Li4,* 1Beijing University of Chinese Medicine, Beijing, People’s Republic of China; 2Department of Rheumatology, Dongfang Hospital Beijing University of Chinese Med
Externí odkaz:
https://doaj.org/article/75e0da8548e84a39ac134df05cfc343d
Autor:
Li Luan, Chengzhi Lv
Publikováno v:
Journal of Dermatological Treatment, Vol 0, Iss 0, Pp 1-16 (2023)
Synovitis, acne, pustulosis, hyperostosis, and osteitis (SAPHO) syndrome is a rare autoinflammatorydisorder without standardized therapy. IL-17 inhibitors have been effective in individual cases. However, some patients with SAPHO may develop psoriasi
Externí odkaz:
https://doaj.org/article/750d985cbac14802926750ef6bdaf366