O'Doherty D S, Schellinger D, Raptopoulos V
J Comput Assist Tomogr. 1977 Oct;1(4):482-6. doi: 10.1097/00004728-197710000-00015.
At present, the diagnosis of pseudohypertrophic muscular dystrophy (PHMD) rests on the clinical picture and the pattern of inheritance and is supported by electrodiagnostic, histologic, and histochemical techniques. In this report we describe the observed computed tomography (CT) changes in six patients with PHMD and compare these abnormal CT scans with scans of the same anatomic region in 16 normal individuals. Scans of patients with polymyositis and sarcoid myopathy are shown for comparison. Two CT patterns, frequently observed in our series, are described.
目前,假肥大性肌营养不良症(PHMD)的诊断基于临床表现和遗传模式,并得到电诊断、组织学和组织化学技术的支持。在本报告中,我们描述了6例PHMD患者的计算机断层扫描(CT)观察结果,并将这些异常CT扫描与16名正常个体相同解剖区域的扫描结果进行比较。还展示了多发性肌炎和结节病性肌病患者的扫描结果以供比较。描述了我们系列中经常观察到的两种CT模式。