Sambrook P, Rickards D, Cumming W J
Department of Radiology, Withington Hospital Manchester, England.
Neuroradiology. 1988;30(6):487-95. doi: 10.1007/BF00339688.
One hundred patients with spinal muscular atrophy (SMA) were assessed by CT scanning using a standardised technique. The spectrum of CT abnormality occurring in SMA was observed and by overall analysis the patients were divided into 4 groups. While the CT appearances of these groups correlated well with clinical assessment of severity of disease, the disease process was usually much more widespread than clinical examination suggested. CT abnormality was first observed in the leg and gluteal muscles, progressing to the posterior spinal, thigh, shoulder girdle and sternomastoid muscles. Hypertrophy of sartorius and gracilis was observed in a significant number of patients. Fascial planes were preserved in involved muscles in over half of the patients, even in late-stage disease. Asymmetrical muscle involvement was seen with increasing frequency as the disease process increased in extent as evaluated by CT scanning. There was no discernible difference in the CT appearances in those patients who clinically had limb-girdle, facioscapulohumeral or scapuloperoneal distribution of weakness.
采用标准化技术对100例脊髓性肌萎缩症(SMA)患者进行CT扫描评估。观察了SMA中出现的CT异常谱,并通过综合分析将患者分为4组。虽然这些组的CT表现与疾病严重程度的临床评估密切相关,但疾病进程通常比临床检查所提示的更为广泛。CT异常首先在腿部和臀肌中观察到,然后发展至脊柱后部、大腿、肩胛带和胸锁乳突肌。在相当数量的患者中观察到缝匠肌和股薄肌肥大。超过半数的患者受累肌肉中的筋膜平面得以保留,即使在疾病晚期也是如此。根据CT扫描评估,随着疾病进程范围的增加,不对称性肌肉受累的出现频率也增加。在临床上有肢带型、面肩肱型或肩胛腓骨型肌无力分布的患者中,CT表现没有明显差异。