Cerebral abnormalities in infants with myelomeningocele

被引:0
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作者
Alexiou, George A. [1 ]
Zarifi, Maria K. [2 ]
Georgoulis, George [1 ]
Mpouza, Eleni [3 ]
Prodromou, Christiana [1 ]
Moutafi, Athina [3 ]
Anagnostakou, Marina [3 ]
Sfakianos, George [1 ]
Prodromou, Neofytos [1 ]
机构
[1] Childrens Hosp Agia Sofia, Dept Neurosurg, Athens, Greece
[2] Childrens Hosp Agia Sofia, Dept Radiol, Athens, Greece
[3] Childrens Hosp Agia Sofia, Dept Neonatol 2, Athens, Greece
关键词
spinal dysraphism; myelomeningocele; MRI; brain; CHIARI-II MALFORMATION; MR-FINDINGS; DECOMPRESSION; HYDROCEPHALUS; ADOLESCENTS; ANOMALIES; CHILDREN;
D O I
暂无
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and purpose: We evaluated brain abnormalities associated with myelomeningocele in infants. Material and methods: Between June 1995 and June 2008, 42 patients with myelomeningocele were treated in our hospital. Only 24 patients (13 males, 11 females, mean age 1.5 months, range 1 day 11 months) were evaluated by both spinal and brain magnetic resonance imaging (MRI) and were enrolled in the study. Results: Brain MRI revealed: hydrocephalus in 21(87.5%) patients, all of whom required immediate shunting. Total agenesis of the corpus callosum was observed in 2 (8.3%) patients, partial agenesis was seen in 4 (17%) patients and 8 (34%) patients had dysplasia of the corpus callosum. Absence of the septum pellucidum was observed in 2 (8%) patients. Widening of the interhemispheric fissure and colpocephaly were noted in 10 (41%) and in 3 (12%) patients, respectively. Abnormal white matter maturation was observed in 2 (8%) patients. Small posterior fossa was observed in 18(74%) patients, Chiari malformation in 16 (67%) patients, cerebellar and brain stem hypoplasia in 3 (12%) and 7 (30%) patients, respectively Conclusions: MRI examination of the myelomeningocele site is not sufficient. Clinicians should consider obtaining imaging studies of the entire neuraxis in patients with myelomeningocele.
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页码:18 / 23
页数:6
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