Campanacci M, Gardini G F, Giunti A, Donati U
Ital J Orthop Traumatol. 1980 Dec;6(3):385-93.
The authors present a study of fifty-seven cases of pseudo-tumoral ossification of the muscles ("circumscribed ossifying myositis") and of the periosteum, supported by clinical, radiographic and histological evidence. This pathological condition is characterised by the formation of hyperplastic bone callus in muscle or periosteum, with a typical radiographic appearance, and with a relationship to trauma. We have excluded from our study pseudo-tumoral periosteal ossification in conditions of congenital origin (osteogenesis imperfecta, neurofibromatosis, Sane et al., 1971; Kullman et al., 1972), hyperplastic fracture callus in cranial trauma, ossification of muscles in limbs which are paretic or paralysed due to cerebral or cord lesions, and hyperplastic fracture callus in congenital syphilis. The form which is the subject of this study is absolutely benign, develops over a period of twelve to twenty-four months, with spontaneous maturation and partial regression. It can abe treated by radiotherapy to accelerate maturation, or by surgery when maturation has been completed.
作者们展示了一项对57例肌肉假瘤样骨化(“局限性骨化性肌炎”)和骨膜假瘤样骨化的研究,该研究有临床、影像学和组织学证据支持。这种病理状况的特征是在肌肉或骨膜中形成增生性骨痂,具有典型的影像学表现,且与创伤有关。我们已将先天性疾病(成骨不全、神经纤维瘤病,Sane等人,1971年;Kullman等人,1972年)中的假瘤样骨膜骨化、颅脑创伤中的增生性骨折骨痂、因脑或脊髓病变导致的肢体瘫痪或麻痹部位肌肉的骨化以及先天性梅毒中的增生性骨折骨痂排除在我们的研究之外。本研究的这种形式绝对是良性的,在12至24个月的时间内发展,具有自发成熟和部分消退的特点。它可以通过放射治疗来加速成熟,或者在成熟完成后通过手术治疗。