Reimao Rubens, Plaggert Paulo G, Adda Carla, Matushita Hamilton, Reed Umbertina C
Pediatric Neurology Section, Department of Neurology, Sao Paulo University Medical School, São Paulo SP, Brazil.
Pediatr Neurol. 2003 Oct;29(4):341-4. doi: 10.1016/s0887-8994(03)00279-0.
Reported is a 4-year-old female with Chiari II malformation and congenital hydrocephalus associated with lumbosacral myelomeningocele who also presented with frontal calvarial foramina depicted by head computed tomographic scans with three-dimensional reconstructions. Magnetic resonance demonstrated bilateral and symmetric frontal lobe malformation-separated-lip clefts schizencephaly-adjacent to the bilateral frontal calvarial foramina. Because the different types of malformations evident in this patient do not share the same developmental origin, the association of findings is unusual and suggests the occurrence of an unknown prenatal factor acting along different stages of central nervous system development.
报告了一名4岁女性,患有Chiari II型畸形和先天性脑积水,伴有腰骶部脊髓脊膜膨出,头部计算机断层扫描三维重建显示其还存在额颅骨孔。磁共振成像显示双侧对称的额叶畸形——分离性唇裂脑裂畸形——毗邻双侧额颅骨孔。由于该患者明显存在的不同类型畸形并非源自同一发育过程,这些发现的关联情况并不常见,提示存在一种未知的产前因素,在中枢神经系统发育的不同阶段发挥作用。