KEGG   DISEASE: 片側巨脳症
エントリ  
H01833                                                             
名称    
片側巨脳症
概要    
Hemimegalencephaly is a rare brain malformation caused by anomalous neuronal and glial proliferation or differentiation, with an abnormally enlarged and dysplastic hemisphere. It can occur as an isolated finding, or as part of a syndrome, such as hypomelanosis of Ito, tuberous sclerosis complex, epidermal nevus syndrome or Klippel-Trenaunay syndrome. Patients have intellectual delay, hemiparesis and severe epilepsy. Drug resistant epilepsy is often treated with a hemispherectomy. If resective surgery is impossible, vagus nerve stimulation (VNS) can be used for seizure palliation. The etiology of hemimegalencephaly is not clear. Some authors consider abnormal neuroepithelial cell lineage as the primary cause.
カテゴリ  
先天奇形
階層分類  
ICD-11 による疾患分類 [BR:jp08403]
 20 発達異常
  主に1つの体系に影響する構造的発達異常
   神経系の構造的発達異常
    LA05  脳の構造的発達異常
     H01833  片側巨脳症
指定難病 [jp08407.html]
 H01833
コメント  
See also H00915 Tuberous sclerosis complex, and H01788 Klippel-Trenaunay-Weber syndrome.
リンク   
ICD-11: LA05.1
ICD-10: Q04.5
MeSH: D065705
文献    
  著者
Ikeda KM, Mirsattari SM
  タイトル
Evolution of epilepsy in hemimegalencephaly from infancy to adulthood: Case report and review of the literature.
  雑誌
Epilepsy Behav Case Rep 7:45-48 (2017)
DOI:10.1016/j.ebcr.2017.02.002
文献    
  著者
Chrastina J, Novak Z, Brazdil M, Hermanova M
  タイトル
Glioblastoma Multiforme in a Patient with Isolated Hemimegalencephaly.
  雑誌
J Neurol Surg Rep 76:e160-3 (2015)
DOI:10.1055/s-0035-1554929
LinkDB    

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