Voigt K, Sauer M, Luthardt T
Pediatr Radiol. 1975 Jan 24;3(1):47-9. doi: 10.1007/BF00973366.
The roentgenological and clinical findings of a five year old girl suffering from cytomegalic inclusion body disease are reported. In this disease unusual circumscript and large calcareous deposits of the basal ganglia and scattered gyriform calcifications of the occipito-parietal cortex were shown on plain skull x-rays and their paraventricular localization demonstrated on pneumoencephalotomogram.
报告了一名患有巨细胞包涵体病的五岁女孩的放射学和临床检查结果。在这种疾病中,普通头颅X光片显示基底节有异常的局限性大钙质沉积,枕顶叶皮质有散在的脑回状钙化,气脑造影显示其位于脑室旁。