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具有单纯溶骨性表现的SAPHO综合征:一例报告。

SAPHO syndrome with a purely osteolytic form: A case report.

作者信息

Kakiuchi Akira, Yamamoto Yayoi, Kanbe Akira, Kojima Daichi, Horikawa Ayumi, Hino Ayako, Doiuchi Tsunehiro, Kurihara Hiroaki

机构信息

Department of Diagnostic and Interventional Radiology, Kanagawa Cancer Center, 2-3-2 Nakao Asahi-ku, Yokohama, Kanagawa, Japan.

出版信息

Radiol Case Rep. 2023 Aug 3;18(10):3612-3614. doi: 10.1016/j.radcr.2023.07.034. eCollection 2023 Oct.

Abstract

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, whereas hyperostosis and osteitis are the most prominent imaging findings. We report the case of a man with osteolytic changes of the lumbar vertebra and a history of palmoplantar pustulosis. Biopsy revealed no neoplasm, suggesting SAPHO syndrome. Our case demonstrates that knowledge of atypical radiologic findings is necessary for the diagnosis of SAPHO syndrome.

摘要

滑膜炎、痤疮、脓疱病、骨肥厚和骨炎(SAPHO)综合征是一种罕见的慢性自身炎症性疾病,可表现出一系列皮肤和骨关节症状。骨质破坏病变并非其特征性表现,而骨肥厚和骨炎是最显著的影像学表现。我们报告一例患有腰椎溶骨性改变且有掌跖脓疱病病史的男性病例。活检未发现肿瘤,提示为SAPHO综合征。我们的病例表明,了解非典型影像学表现对于SAPHO综合征的诊断很有必要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d5a/10415825/9f69f4e0cee1/gr1.jpg

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