Roscam Abbing P J, Hageman G, Willemse J
Brain Dev. 1985;7(5):484-91. doi: 10.1016/s0387-7604(85)80114-5.
CT-scanning of skeletal muscles was performed on 14 patients with arthrogryposis multiplex congenita (AMC), according to an eight-slice protocol. Adipose tissue replacement and atrophy of muscles was found in six patients with neurogenic or myopathic origin of AMC, associated with severe muscle weakness. In the remaining patients with other forms of AMC, in which muscle weakness was less marked or absent, muscular CT-scanning was normal. It is stated that muscular CT-scanning is not a routine investigation in a screening procedure of all cases of AMC. However, CT-scanning appears to be useful in cases of severe AMC with associated muscle weakness in detecting the neurogenic and myopathic forms. It also facilitates the selection of a suitable site for EMG and biopsy and may provide important information for orthopaedic management.
根据八层扫描方案,对14例先天性多发性关节挛缩症(AMC)患者进行了骨骼肌CT扫描。在6例神经源性或肌源性AMC患者中发现了脂肪组织替代和肌肉萎缩,这些患者伴有严重肌无力。在其余其他形式的AMC患者中,肌无力不太明显或不存在,肌肉CT扫描结果正常。研究表明,肌肉CT扫描并非所有AMC病例筛查程序中的常规检查。然而,CT扫描在伴有肌无力的严重AMC病例中,对于检测神经源性和肌源性类型似乎是有用的。它还便于选择合适的肌电图和活检部位,并可为骨科治疗提供重要信息。