Song Xinghua, Sun Wenwen, Meng Zhaowei, Gong Lu, Tan Jian, Jia Qiang, Yu Chunshui, Yu Tielian
Department of Nuclear Medicine, Tianjin Medical University General Hospital, Tianjin 300052, P.R.China.
Department of Rheumatology and Immunological Diseases, Tianjin Medical University General Hospital, Tianjin 300052, P.R.China.
Exp Ther Med. 2014 Aug;8(2):419-422. doi: 10.3892/etm.2014.1758. Epub 2014 Jun 4.
The present study reports a rare case of synovitis, acne, pustulosis, hyperostosis and osteitis (SAPHO) syndrome in an adult male. The 42-year-old man complained of skin lesions, chest pain and lumbago. Laboratory evaluations demonstrated an elevated erythrocyte sedimentation rate and increased levels of C-reactive protein. Computerized tomography, bone scintigraphy and magnetic resonance imaging revealed multiple bone lesions. A diagnosis of SAPHO syndrome was made. Non-steroidal anti-inflammatory drugs, alendronate sodium and steroids were administered, which resulted in clinical improvement. The current case study demonstrates that skin manifestation and multiple imaging modalities are important in generating a definite diagnosis of SAPHO syndrome, and that early treatment is vital for a positive outcome.
本研究报告了一例成年男性患滑膜炎、痤疮、脓疱病、骨肥厚和骨炎(SAPHO)综合征的罕见病例。这名42岁的男子主诉有皮肤病变、胸痛和腰痛。实验室检查显示红细胞沉降率升高和C反应蛋白水平升高。计算机断层扫描、骨闪烁显像和磁共振成像显示有多处骨病变。确诊为SAPHO综合征。给予非甾体抗炎药、阿仑膦酸钠和类固醇治疗后,临床症状有所改善。当前的病例研究表明,皮肤表现和多种成像方式对于明确诊断SAPHO综合征很重要,并且早期治疗对于取得良好预后至关重要。