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Advisor(s)
Abstract(s)
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.
Description
Keywords
Acquired Hyperostosis Syndrome / diagnosis* Acquired Hyperostosis Syndrome / drug therapy* Adult Female Male HCC IMA HCC DAUTOIM Humans Acquired Hyperostosis Syndrome / immunology Antibodies, Monoclonal, Humanized / therapeutic use Bone and Bones / diagnostic imaging* Middle Aged Radionuclide Imaging Treatment Outcome Tumor Necrosis Factor Inhibitors / therapeutic use* Ustekinumab / therapeutic use
Citation
Clin Rheumatol . 2020 Jan;39(1):177-187
Publisher
Springer