SAPHO Syndrome: About Three Cases and Review of the Literature

Abba Abbasse, N. Moustapha, D. L. Mohamed, Ali Hassan
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引用次数: 0

Abstract

Background: SAPHO syndrome (synovitis, acne, pustulosis, hyperostosis, osteitis) is both a dermatological and a rheumatological entity, with the common denominator of an aseptic inflammatory process, the bone manifestations of which are the essential element of the diagnosis. Despite its chronic and recurrent nature, SAPHO syndrome is very rarely the cause of major disability, even after several decades of evolution. Objective: We want to illustrate through three clinical cases, the importance of the anamnesis, the clinic, the diagnostic criteria in the diagnosis of SAPHO syndrome. Presentation of the cases: We studied the clinical file of three patients consulted in the Rheumatology Department of the CHU Aristide LeDantec in Dakar, Senegal, between January 2012 and December 2020, suffering from SAPHO syndrome of diagnosis established in accordance with the diagnostic criteria of SAPHO syndrome proposed by Khan et al. of 1994. Conclusion: SAPHO syndrome is a rare pathological entity, over a period of 8 years we report 3 cases.
SAPHO综合征3例及文献复习
背景:SAPHO综合征(滑膜炎、痤疮、脓疱病、骨质增生、骨炎)既是一种皮肤病,也是一种风湿病,其共同点是无菌性炎症过程,其骨骼表现是诊断的基本要素。尽管SAPHO综合征具有慢性和复发性,但即使经过几十年的进化,它也很少成为严重残疾的原因。目的:通过三例临床病例,阐明SAPHO综合征的记忆、临床及诊断标准的重要性。病例介绍:我们研究了2012年1月至2020年12月在塞内加尔达喀尔CHU Aristide LeDantec风湿病科咨询的三名患者的临床档案,他们患有根据Khan等人1994年提出的SAPHO综合征诊断标准确定的SAPHO综合症。结论:SAPHO综合征是一种罕见的病理实体,我们在8年的时间里报告了3例。
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来源期刊
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