Tyler Philippa, Saifuddin Asif
Department of Radiology, The Royal National Orthopaedic Hospital, Middlesex, United Kingdom.
Semin Musculoskelet Radiol. 2010 Jun;14(2):201-16. doi: 10.1055/s-0030-1253161. Epub 2010 May 18.
Myositis ossificans (MO) is characterized by abnormal heterotopic bone formation involving striated muscle, tendons, ligaments, fasciae, and aponeuroses. Myocardium, the diaphragm, tongue, larynx, smooth muscle, and sphincters are all spared. Several subtypes of myositis ossificans exist: posttraumatic myositis ossificans (PTMO), nontraumatic/pseudomalignant myositis ossificans, and myositis ossificans progressiva (MOP). This article reviews the clinical features and differential diagnoses of each subtype of MO and illustrates the typical imaging features demonstrated by plain radiography, ultrasound, radionuclide bone scans, computed tomography, and magnetic resonance imaging.
骨化性肌炎(MO)的特征是在横纹肌、肌腱、韧带、筋膜和腱膜中出现异常的异位骨形成。心肌、膈肌、舌、喉、平滑肌和括约肌均不受累。骨化性肌炎有几种亚型:创伤后骨化性肌炎(PTMO)、非创伤性/假性恶性骨化性肌炎和进行性骨化性肌炎(MOP)。本文综述了MO各亚型的临床特征和鉴别诊断,并阐述了X线平片、超声、放射性核素骨扫描、计算机断层扫描和磁共振成像所显示的典型影像学特征。