SAPHO syndrome in the mandible: A 17-patient-based experience

IF 2 3区 医学 Q2 DENTISTRY, ORAL SURGERY & MEDICINE Journal of Stomatology Oral and Maxillofacial Surgery Pub Date : 2025-02-01 DOI:10.1016/j.jormas.2024.102027
Zhuoying Cai , Yanming Liu , Jing Xue , Di He , Menghua Yu , Qin Yan , Yihang Sun
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Abstract

SAPHO (Synovitis, Acne, Pustulosis, Hyperostosis and Osteitis) syndrome is a rare inflammatory bone disorder with a remarkably low incidence. The condition's impact on the mandible is exceptionally uncommon, often resulting in a high rate of misdiagnosis and an extended duration of illness. The objective of this study was to assess patients with SAPHO syndrome in the mandible in across various stages and to dissect their distinctive features, aiming to provide future clinical experience for the disease.
Methods: A retrospective analysis was performed on a cohort of 17 patients diagnosed with SAPHO syndrome affecting the mandible at the Second Affiliated Hospital of Zhejiang University from January 2020 to March 2023. Data including clinical presentations, imaging characteristics, and laboratory results were collected.
Results: The median age at disease onset was 25, with a diagnostic interval of 26 months. Notably, seven individuals were prepubescent (under the age of 14). Seven patients (41.18 %) exhibited polyostotic involvement, while eight patients (47.06 %) presented with dermatological manifestations either concurrently with or subsequent to the osseous lesions. Condyle involvement was identified in six patients (35.29 %), and bilateral mandibular affection was noted in an equivalent number. The majority of patients (sixteen patients, 94.12 %) reported symptomatic relief following treatment with nonsteroidal anti-inflammatory drugs (NSAIDs). Glucocorticoids were instrumental in managing severe pain and extreme limitations in mouth opening. For patients with refractory disease, tumor necrosis factor-alpha (TNF-α) inhibitors, Janus kinase (JAK) inhibitors and bisphosphonates were employed. Ultimately, effective pain management was achieved in the entire cohort.
Conclusion: The diagnosis of SAPHO syndrome involving the mandible is exclusionary. It is important to improve diagnostic accuracy among oral and maxillofacial surgeons (OMFS), dentists, and rheumatologists to avoid unnecessary surgery and tooth extraction. TNF-α inhibitors, JAK inhibitors and bisphosphonates are recommended as third-line drugs.
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下颌骨 SAPHO 综合征:基于 17 位患者的经验。
SAPHO(滑膜炎、痤疮、脓疱病、骨质增生和骨炎)综合征是一种罕见的炎症性骨病,发病率极低。该病对下颌骨的影响异常罕见,往往导致误诊率高和病程延长。本研究的目的是评估下颌骨SAPHO综合征患者在不同阶段的表现,并剖析其显著特征,旨在为该疾病提供未来的临床经验:对浙江大学附属第二医院2020年1月至2023年3月期间确诊的17例下颌骨SAPHO综合征患者进行回顾性分析。收集的数据包括临床表现、影像学特征和实验室结果:中位发病年龄为 25 岁,诊断间隔为 26 个月。值得注意的是,7 名患者为青春期前(14 岁以下)。7名患者(41.18%)表现为多骨质受累,8名患者(47.06%)在骨质病变的同时或之后出现皮肤病表现。六名患者(35.29%)的髁状突受累,双侧下颌骨受累的人数相当。大多数患者(16 人,94.12%)在接受非甾体抗炎药(NSAIDs)治疗后症状得到缓解。糖皮质激素有助于缓解剧烈疼痛和张口极度受限。对于难治性疾病患者,则使用肿瘤坏死因子-α(TNF-α)抑制剂、Janus 激酶(JAK)抑制剂和双膦酸盐。最终,所有患者都得到了有效的疼痛控制:结论:下颌骨SAPHO综合征的诊断具有排除性。提高口腔颌面外科医生(OMFS)、牙科医生和风湿病学家的诊断准确性以避免不必要的手术和拔牙非常重要。建议将 TNF-α 抑制剂、JAK 抑制剂和双磷酸盐作为三线药物。
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来源期刊
Journal of Stomatology Oral and Maxillofacial Surgery
Journal of Stomatology Oral and Maxillofacial Surgery Surgery, Dentistry, Oral Surgery and Medicine, Otorhinolaryngology and Facial Plastic Surgery
CiteScore
2.30
自引率
9.10%
发文量
0
审稿时长
23 days
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