Zee C S, McComb J G, Segall H D, Tsai F Y, Stanley P
J Comput Assist Tomogr. 1981 Apr;5(2):201-5. doi: 10.1097/00004728-198104000-00011.
Using computed tomography (CT), we have been able to identify the combined occurrence of lipoma of the corpus callosum and dysraphic lesions associated with frontal bone defects in two cases. In one case, there was a true encephalocele, and in the other case a lipoma with cartilaginous tissue was present. Such combinations are very rare; thus, the impetus to report these cases. The disorganization of the central nervous system was extensive in the first infant and was associated with profound developmental delay, while the second infant had much less anatomical abnormality, and development to date is normal. Bony defects (on skull films), typical appearances of lipoma of the corpus callosum, and characteristics of the dysraphic lesions (on CT) were seen. Angiography was obtained in the infant with a true encephalocele.
通过计算机断层扫描（CT），我们在两例病例中发现了胼胝体脂肪瘤与伴有额骨缺损的神经管闭合不全性病变同时存在的情况。在其中一例中，存在真正的脑膨出，而在另一例中则有含软骨组织的脂肪瘤。这种组合非常罕见；因此，有动力报告这些病例。第一例婴儿的中枢神经系统紊乱广泛，且伴有严重发育迟缓，而第二例婴儿的解剖学异常则少得多，迄今为止发育正常。观察到了（颅骨平片上的）骨缺损、胼胝体脂肪瘤的典型表现以及（CT上的）神经管闭合不全性病变特征。对患有真正脑膨出的婴儿进行了血管造影。
