Clinical characteristics of epileptic seizure in neurofibromatosis type 1 in 15 cases.
10.3760/cma.j.cn112140-20230829-00146
- Author:
Fan WU
1
;
Xin Na JI
1
;
Meng Xiao SHEN
1
;
Shuo FENG
1
;
Li Na XIE
1
;
Yan Yan GAO
1
;
Shu Pin LI
1
;
Ai Yun YANG
2
;
Jian Hua WANG
2
;
Qian CHEN
1
;
Xue ZHANG
3
Author Information
1. Department of Neurology, Children's Hospital Capital Institute of Pediatrics, Beijing 100020, China.
2. Translational Medicine Laboratory, Beijing Key Laboratory of Child Development and Nutriomics, Capital Institute of Pediatrics, Beijing 100020, China.
3. Department of Medical Genetics, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences, School of Basic Medicine, Peking Union Medical College, Beijing 100730, China.
- Publication Type:Journal Article
- MeSH:
Male;
Female;
Humans;
Child, Preschool;
Child;
Neurofibromatosis 1/diagnosis*;
Retrospective Studies;
Intellectual Disability;
Electroencephalography;
Epilepsy/etiology*;
Seizures/etiology*
- From:
Chinese Journal of Pediatrics
2023;61(12):1124-1128
- CountryChina
- Language:Chinese
-
Abstract:
Objective: To summarize the clinical characteristics of epileptic seizure associated with neurofibromatosis type 1 (NF1). Methods: 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. Results: 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. Conclusions: 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.
