Unidade de Doenças Auto-imunes/Serviço Medicina 7.2, Hospital de Curry Cabral, Centro Hospitalar Universitário de Lisboa Central, Lisbon, Portugal.
Serviço de Medicina IV, Hospital de Santarém EPE, Av. Bernardo Santareno, 2005-177, Santarém, Portugal.
Clin Rheumatol. 2020 Jan;39(1):177-187. doi: 10.1007/s10067-019-04675-2. Epub 2019 Jul 16.
SAPHO (synovitis, acne, pustulosis, hyperostosis and osteitis) syndrome is a heterogeneous condition combining osteoarticular and cutaneous manifestations. Conventional treatments are mostly ineffective. We hereby report two patients, the first with an aggressive form of disease and the second with an incomplete response to two different anti-TNF-α agents. Both were successfully treated with tocilizumab and ustekinumab, respectively, over a long period of time. A narrative review of a biological therapy in SAPHO syndrome yielded very little information on the specific use of these agents. We highlight the advantages of personalising therapy and describe emerging promising treatments for this disease.
SAPHO(滑膜炎、痤疮、脓疱病、骨肥厚和骨炎)综合征是一种异质性疾病,结合了骨和关节及皮肤表现。常规治疗大多无效。我们在此报告两例患者,一例疾病表现为侵袭性,另一例对两种不同的抗 TNF-α 药物反应不完全。两例患者均分别长期接受托珠单抗和乌司奴单抗治疗,取得了成功。对 SAPHO 综合征的生物治疗进行叙述性综述,结果发现关于这些药物具体使用的信息很少。我们强调了个体化治疗的优势,并描述了这种疾病的新兴有前途的治疗方法。