Okuno Hiroshi, Watanuki Munenori, Kuwahara Yoshiyuki, Sekiguchi Akira, Mori Yu, Hitachi Shin, Miura Keiki, Ogura Ken, Watanabe Mika, Hosaka Masami, Hatori Masahito, Itoi Eiji, Sato Katsumi
a Department of Orthopaedic Surgery , Tohoku Rosai Hospital , Sendai , Japan.
b Department of Orthopaedic Surgery , Tohoku University Hospital , Sendai , Japan.
Mod Rheumatol. 2018 Jul;28(4):703-708. doi: 10.1080/14397595.2017.1372874. Epub 2017 Sep 21.
The purpose of this study was to facilitate the understanding of the SAPHO (Synovitis, Acne, Pustulosis, Hyperostosis, and Osteitis) syndrome by analyzing the clinical and radiological features of 67 Japanese patients with SAPHO syndrome.
Sixty-seven Japanese patients (female/male: 44/23, mean age at onset: 48.5 years) were diagnosed with SAPHO syndrome from 2002 to 2013 at our hospital. Medical records and radiological imaging of these patients were retrospectively reviewed.
Among the 67 patients, 41 had dermatological manifestations, such as palmoplantar pustulosis, acne, and psoriasis. Initial symptom was local pain in all patients, and the most common initial site of the symptom was the anterior chest. Bacterial and fungal cultures from 20 bone biopsies were all negative. Histopathological diagnosis of the specimens was non-specific inflammation in all cases. Bone lesions were observed in 65 patients (97.0%). On the other hand, articular lesions including enthesitis were found in 31 patients (46.2%).
SAPHO syndrome had different clinical and radiological aspects. The clinical features were not remarkable, except the dermatological manifestations and the involvement of the anterior chest. Bone lesions including hyperostosis and osteitis were found radiographically in the majority of patients with SAPHO syndrome. These are the characteristics of the SAPHO syndrome, with the exclusion of other bone diseases.
本研究旨在通过分析67例日本SAPHO(滑膜炎、痤疮、脓疱病、骨肥厚和骨炎)综合征患者的临床和放射学特征,促进对该综合征的理解。
2002年至2013年期间,我院确诊了67例日本患者(女性/男性:44/23,平均发病年龄:48.5岁)患有SAPHO综合征。对这些患者的病历和放射影像学资料进行了回顾性分析。
67例患者中,41例有皮肤表现,如掌跖脓疱病、痤疮和银屑病。所有患者的初始症状均为局部疼痛,最常见的初始症状部位是前胸。20例骨活检的细菌和真菌培养均为阴性。所有病例标本的组织病理学诊断均为非特异性炎症。65例患者(97.0%)观察到骨病变。另一方面,31例患者(46.2%)发现有关节病变,包括附着点炎。
SAPHO综合征有不同的临床和放射学表现。除皮肤表现和前胸受累外,临床特征并不显著。大多数SAPHO综合征患者在影像学上发现有包括骨肥厚和骨炎在内的骨病变。这些是SAPHO综合征的特征,可排除其他骨病。