Zajac Anna, Herman-Sucharska Izabela, Kroczka Sławomir, Kubik Alicja, Nardzewska-Szczepanik Monika
Klinika Neurologii Dzieciecej, Uniwersytetu Jagiellońskiego, Collegium Medicum, Kraków.
Przegl Lek. 2007;64(11):942-5.
Diagnosis of primary generalised seizures may be not precise because difficulties exist with the assessment of information of focal onset of these seizures.
The aim was to examine if the careful searching for partial component of seizures is necessary in children with so called primary generalized seizures.
The examined group included 45 children aged 6 month to 18 year (mean 11 year) within 19 girls and 26 boys, hospitalized during the year 2006 in the Department of Pediatric Neurology UJ CM in Krakow. The history indicated the primary generalized character of seizures. The tonic-clonic seizures were observed in 39 children, myoclonic in 3, infantile spasms in 1 and absence in other 2. In 6 patients familiar epilepsy was diagnosed in first-degree cousins. Neuropediatric examination was normal apart from 4 children with dysmorphic features of the face. Intellectual development was normal in 43 children, however it was close to the lower range in one and mildly delayed in the other one. Generalized paroxysmal bioelectric activity was detected in 43 children and in 2 children EEG pattern was normal. MRI was performed in SE T1, FSE T2, PD, FLAIR and IR T1 sequences with 3 or 5 millimetre thickness of layer in the sagital, coronal and transversal plane, using a 1.5 T signa horizon HiSpeed General Electric. These examinations were performed in the Voxel MR Laboratory in University Children's Hospital in Krakow.
MRI results were normal in 14/45 children and in others pathological. In 9/45 MR revealed subarachnoidal cyst, in 8 lateral ventricles asymmetry, in 5 mild demyelination, in 9 subarachnoid space and lateral ventricles dilatation. In 2/45 children brain tumors (hamartoma of the hypothalamus and DNET of the temporal lobe), in 1 gliosis of the occipital lobe were revealed, however other insignificant changes were also observed. Dual or multiple MRI pathology was revealed in 14 children. In17/45 children abnormalities were localized.
Existence of focal pathology in MRI of 38% children with the history of so called primary generalized seizures suggested the necessity of more careful searching for partial component of seizures.
原发性全身性癫痫发作的诊断可能并不精确,因为评估这些发作的局灶性起始信息存在困难。
目的是研究对于所谓原发性全身性癫痫发作的儿童,仔细寻找发作的局灶性成分是否必要。
研究组包括2006年在克拉科夫雅盖隆大学医学院儿科神经科住院的45名年龄在6个月至18岁(平均11岁)的儿童,其中19名女孩,26名男孩。病史显示癫痫发作具有原发性全身性特征。39名儿童观察到强直阵挛发作,3名儿童为肌阵挛发作,1名儿童为婴儿痉挛发作,另外2名儿童为失神发作。6名患者在一级亲属中被诊断出家族性癫痫。除4名面部有畸形特征的儿童外,神经儿科检查均正常。43名儿童智力发育正常,然而有1名儿童接近低限,另1名儿童轻度延迟。43名儿童检测到全身性阵发性生物电活动,2名儿童脑电图模式正常。使用1.5T Signa Horizon HiSpeed通用电气公司的设备,在矢状面、冠状面和横断面以3或5毫米层厚进行SE T1、FSE T2、PD、FLAIR和IR T1序列的MRI检查。这些检查在克拉科夫大学儿童医院的体素MR实验室进行。
45名儿童中14名MRI结果正常,其他为病理性结果。45名中有9名MR显示蛛网膜下囊肿,8名显示侧脑室不对称,5名显示轻度脱髓鞘,9名显示蛛网膜下腔和侧脑室扩张。2名儿童发现脑肿瘤(下丘脑错构瘤和颞叶神经上皮肿瘤),1名儿童发现枕叶胶质增生,然而也观察到其他不显著变化。14名儿童显示双重或多重MRI病变。45名中有17名儿童病变定位。
38%有所谓原发性全身性癫痫发作病史的儿童MRI存在局灶性病变,提示有必要更仔细地寻找发作的局灶性成分。