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Mandibular Osteitis Leading to the Diagnosis of SAPHO Syndrome

机译:下颌骨炎导致SAPHO综合征的诊断

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摘要

Synovitis, acne, pustulosis, hyperostosis, and osteitis (SAPHO) syndrome is a disorder characterized by pustular skin lesions and osteoarticular lesions. Mandibular involvement of SAPHO syndrome is clinically rare, and it is difficult to reach a diagnosis of SAPHO syndrome from only mandibular manifestations. This report describes the case of a 26-year-old woman who presented with mandibular osteitis. Orthopantomogram and computed tomography showed sclerotic change of the right body of the mandible with periosteal reaction without odontogenic infection, which suggested the possibility of SAPHO syndrome. Detailed medical interview found that she had a history of palmoplantar pustulosis treated at a local dermatology clinic and additional bone scintigraphy showed diffuse increased uptake in the right mandible, as well as in the sternum and the sternocostoclavicular joints. She was eventually diagnosed as having SAPHO syndrome. We should consider SAPHO syndrome when we encounter a patient with mandibular osteitis of unknown etiology.
机译:滑膜炎,痤疮,脓疱病,肥大和骨炎(SAPHO)综合征是一种以脓疱性皮肤病变和骨关节病变为特征的疾病。 SAPHO综合征的下颌受累在临床上很少见,仅靠下颌表现很难诊断出SAPHO综合征。该报告描述了一名26岁女性下颌骨炎的病例。正射影像和计算机断层扫描显示下颌骨的右半部发生硬化变化,并伴有骨膜反应而无牙源性感染,这提示SAPHO综合征的可能性。详细的医学访谈发现她有在当地皮肤病学诊所接受治疗的掌plant脓疱病的病史,另外的骨闪烁显像显示右下颌骨,胸骨和胸锁骨关节的摄取呈弥漫性增加。她最终被诊断出患有SAPHO综合征。当遇到病因不明的下颌骨炎患者时,应考虑SAPHO综合征。

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