Wu F, Ji X N, Shen M X, Feng S, Xie L N, Gao Y Y, Li S P, Yang A Y, Wang J H, Chen Q, Zhang X
Department of Neurology, Children's Hospital Capital Institute of Pediatrics, Beijing 100020, China.
Translational Medicine Laboratory, Beijing Key Laboratory of Child Development and Nutriomics, Capital Institute of Pediatrics, Beijing 100020, China.
Zhonghua Er Ke Za Zhi. 2023 Dec 2;61(12):1124-1128. doi: 10.3760/cma.j.cn112140-20230829-00146.
To summarize the clinical characteristics of epileptic seizure associated with neurofibromatosis type 1 (NF1). From January 2017 to July 2023 at Children's Hospital Capital Institute of Pediatrics, medical records of patients with both NF1 and epileptic seizure were reviewed in this case series study. The clinical characteristics, treatment and prognosis were analyzed retrospectively. A total of 15 patients(12 boys and 3 girls) were collected. Café-au-lait macules were observed in all 15 patients. There were 6 patients with neurodevelopmental disorders and the main manifestations were intellectual disability or developmental delay. The age at the first epileptic seizure was 2.5 (1.2, 5.5) years. There were various seizure types, including generalized tonic-clonic seizures in 8 patients, focal motor seizures in 6 patients, epileptic spasm in 4 patients, tonic seizures in 1 patient, absence in 1 patient, generalized myoclonic seizure in 1 patient and focal to bilateral tonic-clonic seizure in 1 patient. Among 14 patients whose brain magnetic resonance imaging results were available, there were abnormal signals in corpus callosum, basal ganglia, thalamus or cerebellum in 6 patients, dilated ventricles of different degrees in 3 patients, blurred gray and white matter boundary in 2 patients, agenesis of corpus callosum in 1 patient and no obvious abnormalities in the other patients. Among 13 epilepsy patients, 8 were seizure-free with 1 or 2 antiseizure medications(ASM), 1 with drug resistant epilepsy was seizure-free after left temporal lobectomy, and the other 4 patients who have received 2 to 9 ASM had persistent seizures. One patient with complex febrile convulsion achieved seizure freedom after oral administration of diazepam on demand. One patient had only 1 unprovoked epileptic seizure and did not have another seizure without taking any ASM. The first epileptic seizure in NF1 patients usually occurs in infancy and early childhood, with the main seizure type of generalized tonic-clonic seizure and focal motor seizure. Some patients have intellectual disability or developmental delay. Most epilepsy patients achieve seizure freedom with ASM.
总结1型神经纤维瘤病(NF1)相关癫痫发作的临床特征。在本病例系列研究中,回顾了2017年1月至2023年7月在首都儿科研究所附属儿童医院就诊的NF1合并癫痫发作患者的病历。对其临床特征、治疗及预后进行回顾性分析。共收集15例患者(12例男性,3例女性)。15例患者均观察到牛奶咖啡斑。6例患者有神经发育障碍,主要表现为智力残疾或发育迟缓。首次癫痫发作年龄为2.5(1.2,5.5)岁。癫痫发作类型多样,包括8例全身强直-阵挛发作、6例局灶性运动发作、4例癫痫性痉挛、1例强直发作、1例失神发作、1例全身肌阵挛发作和1例从局灶性发作进展为双侧强直-阵挛发作。在14例有脑部磁共振成像结果的患者中,6例胼胝体、基底节、丘脑或小脑有异常信号,3例有不同程度的脑室扩张,2例灰白质边界模糊,1例胼胝体发育不全,其余患者无明显异常。13例癫痫患者中,8例使用1或2种抗癫痫药物(ASM)后无癫痫发作,1例药物难治性癫痫患者在左颞叶切除术后无癫痫发作,另外4例接受2至9种ASM治疗的患者仍有癫痫发作。1例复杂性热性惊厥患者按需口服地西泮后无癫痫发作。1例患者仅发作1次自发性癫痫,未服用任何ASM未再发作。NF1患者首次癫痫发作通常发生在婴幼儿期,主要发作类型为全身强直-阵挛发作和局灶性运动发作。部分患者有智力残疾或发育迟缓。大多数癫痫患者使用ASM可实现无癫痫发作。