萨福综合征
医学
脓疱病
阿达木单抗
坏疽性脓皮病
骨质增生
化脓性汗腺炎
骨炎
皮肤病科
掌跖脓疱病
滑膜炎
外科
英夫利昔单抗
关节炎
类风湿性关节炎
骨髓炎
病理
内科学
银屑病
肿瘤坏死因子α
疾病
作者
Dunja Ana Vekic,Jane Woods,Peter Lin,Geoffrey D. Cains
摘要
Abstract SAPHO (synovitis, acne, pustulosis, hyperostosis, and osteitis) syndrome is a rare inflammatory condition describing the combination of skin, bone, and joint manifestations that has a heterogeneous presentation. We report a case of severe SAPHO syndrome in association with hidradenitis suppurativa and pyoderma gangrenosum in a 27‐year‐old male. The patient had an initial migratory arthritis affecting the knees, ankles, metacarpophalangeal joints, proximal interphalangeal joints, wrists, shoulder, and lower back, which progressed to a persistent arthritis and swelling at the sternum, shoulders, wrists, hands, feet, and lower back. Radiographic changes were consistent with the diagnosis of SAPHO syndrome. Serum proinflammatory cytokine levels were significantly elevated and improved substantially after 3 months of therapy. Rationale for therapy in this patient was the observation that tumor necrosis alpha antagonists have been successfully used in SAPHO syndrome, and since arthropathy was so prominent in our patient, we elected to use adalimumab combined with methotrexate.
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