| Literature DB >> 31312988 |
Adelaide Sofia Batalha Figueiredo1,2, Ana Luísa Oliveira3,4, António Caetano5, Maria Francisca Moraes-Fontes3.
Abstract
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.Entities:
Keywords: Anti-IL-1 agents; Anti-IL-12/IL-23 agents; Anti-IL-6 agents; Anti-TNF-α agents; SAPHO syndrome; Treatment
Year: 2019 PMID: 31312988 DOI: 10.1007/s10067-019-04675-2
Source DB: PubMed Journal: Clin Rheumatol ISSN: 0770-3198 Impact factor: 2.980