Seizures in paediatric Chiari type I malformation: the role of singlephoton emission computed tomography

被引:10
|
作者
Iannetti, P
Spalice, A
Ciccoli, CD
Bruni, O
Festa, A
Maini, CL
机构
[1] Univ Roma La Sapienza, Dept Dev Neurol & Psychiat, IT-00161 Rome, Italy
[2] Regina Elena Hosp, Dept Nucl Med, Rome, Italy
[3] Univ Roma La Sapienza, Dept Pediat, Div Pediat Neurol, IT-00161 Rome, Italy
关键词
Chiari I malformation; hypoperfusion; microdysgenesis; seizures; SPECT;
D O I
10.1080/08035250252833987
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Chiari type I malformation is one of the posterior fossa maldevelopments with which different clinical manifestations have been associated. Seizures have only recently been associated with Chiari type I malformation, This study reports on 4 children with epilepsy (2M, 217; age range 815 y) diagnosed with Chiari type I malformation by brain magnetic resonance imaging (MRI), in whom no cortical structural involvement was observed. In these patients an interictal ethylcysteinate-dimer-single-photon emission computed tomographic (ECD-SPECT) study was performed to define more precisely the relationship between Chiari type I malformation and seizures. In these patients the hypoperfusion area correlated with electroencephalographic (EEG) focal abnormalities. These hypoperfusions may represent the functional aspect of a cerebral microdysgenesis; seizures and EEG epileptic anomalies may also be linked to the complex network connection between cortices and cerebellar hemispheres. A cerebellar hypoperfusion was also detected in two of the four examined patients, indicating a functional or structural involvement. Conclusion: Interictal SPECT scans are helpful for the clarification of seizures in patients with Chiari type I malformation.
引用
收藏
页码:313 / 317
页数:5
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