Yoshioka M, Saiwai S
Department of Pediatrics, Kobe General Hospital, Japan.
Brain Dev. 1988;10(1):41-4. doi: 10.1016/s0387-7604(88)80044-5.
Sixty-two computed tomographic (CT) scans of 36 patients with congenital muscular dystrophy of Fukuyama type (FCMD) were analysed. A low density area in the cerebral white matter was characteristic of FCMD and a special reference was made to the changes in the white matter low density. It was present in 15 patients out of 36 (42%) and frequently seen in the scans obtained on the younger patients; among 11 scans taken of patients between 1 and 2 years of age, 10 scans (91%) showed the white matter low density. Repeated CT scans were carried out on 26 of the 36 cases. Follow-up study revealed that the white matter low density areas were most apparent around the age of one year and decreased or disappeared at 2 or 3 years of age. From these observations, delayed myelination was suspected for the pathogenesis of the low density area found in FCMD.
对36例福山型先天性肌营养不良(FCMD)患者的62份计算机断层扫描(CT)进行了分析。大脑白质中的低密度区是FCMD的特征,特别提及了白质低密度的变化。36例患者中有15例(42%)出现这种情况,且在较年轻患者的扫描中经常见到;在1至2岁患者的11份扫描中,10份扫描(91%)显示有白质低密度。对36例中的26例进行了重复CT扫描。随访研究显示,白质低密度区在1岁左右最为明显,在2或3岁时减少或消失。基于这些观察结果,怀疑延迟髓鞘形成是FCMD中发现的低密度区的发病机制。