Kransdorf M J, Temple H T, Sweet D E
Department of Radiology, Saint Mary's Hospital, Richmond, VA 23226, USA.
Skeletal Radiol. 1998 May;27(5):283-7. doi: 10.1007/s002560050382.
Focal myositis is a pseudotumor of soft tissue that typically occurs in the deep soft tissue of the extremities, and is a relatively rare lesion. There is a wide clinical spectrum, with approximately one-third of patients with focal myositis subsequently developing polymyositis, and clinical symptoms of generalized weakness, fever, myalgia, and weight loss, with elevation of creatine phosphokinase. We report the case of a patient with focal myositis who subsequently developed myositis ossificans-like features.
局灶性肌炎是一种软组织假瘤,通常发生于四肢深部软组织,是一种相对罕见的病变。其临床谱广泛,约三分之一的局灶性肌炎患者随后会发展为多发性肌炎,伴有全身无力、发热、肌痛和体重减轻等临床症状,同时肌酸磷酸激酶升高。我们报告一例局灶性肌炎患者,该患者随后出现了骨化性肌炎样特征。