Jacquemin C, Mullaney P, Bosley T M
Radiology Department, King Khaled Eye Specialist Hospital, PO Box 7191, Riyadh 11462, Saudi Arabia.
Neuroradiology. 2001 Feb;43(2):178-82. doi: 10.1007/s002340000455.
We report two patients with abnormal development of the lesser wing of the sphenoid bone, globe, optic nerve and cerebral hemisphere without stigmata of neurofibromatosis type 1. The lesser wing of the sphenoid bone was abnormally formed and was not ossified ipsilateral to the dysmorphic eye and underdeveloped cerebral hemisphere. Maldevelopment of the sphenoid wing may interfere with the normal closure of the optic vesicle and normal growth of encephalic structures, possibly by disturbing developmental tissue interactions. These patients may exhibit a type of restricted primary sphenoid dysplasia, while the sphenoid dysplasia of neurofibromatosis type 1 may be secondary to orbital or ocular neurofibromas and other factors associated with that disease.
我们报告了两名蝶骨小翼、眼球、视神经和大脑半球发育异常但无1型神经纤维瘤病体征的患者。蝶骨小翼形成异常,在同侧眼球畸形和大脑半球发育不全的情况下未发生骨化。蝶骨翼发育不良可能会干扰视泡的正常闭合和脑结构的正常生长,可能是通过扰乱发育组织间的相互作用。这些患者可能表现出一种局限性原发性蝶骨发育异常,而1型神经纤维瘤病的蝶骨发育异常可能继发于眼眶或眼部神经纤维瘤以及与该疾病相关的其他因素。