Management of Chiasmatic-Hypothalamic Gliomas in Children

소아 시교차-시상하부 신경교종의 치료

  • Doh, Hong-Jik (Department of Neurosurgery, Keimyung University School of Medicine Dongsan Medical Center) ;
  • Kim, Il-Man (Department of Neurosurgery, Keimyung University School of Medicine Dongsan Medical Center) ;
  • Lee, Chang Young (Department of Neurosurgery, Keimyung University School of Medicine Dongsan Medical Center) ;
  • Son, Eun Ik (Department of Neurosurgery, Keimyung University School of Medicine Dongsan Medical Center) ;
  • Kim, Dong Won (Department of Neurosurgery, Keimyung University School of Medicine Dongsan Medical Center) ;
  • Yim, Man Bin (Department of Neurosurgery, Keimyung University School of Medicine Dongsan Medical Center) ;
  • Kim, Sang Pyo (Department of Pathology, Keimyung University School of Medicine Dongsan Medical Center)
  • 도홍직 (계명대학교 의과대학 동산의료원 신경외과학교실) ;
  • 김일만 (계명대학교 의과대학 동산의료원 신경외과학교실) ;
  • 이창영 (계명대학교 의과대학 동산의료원 신경외과학교실) ;
  • 손은익 (계명대학교 의과대학 동산의료원 신경외과학교실) ;
  • 김동원 (계명대학교 의과대학 동산의료원 신경외과학교실) ;
  • 임만빈 (계명대학교 의과대학 동산의료원 신경외과학교실) ;
  • 김상표 (계명대학교 의과대학 동산의료원 병리학교실)
  • Received : 2001.05.14
  • Accepted : 2001.07.12
  • Published : 2001.09.28

Abstract

Objective : Management strategies for pediatric chiasmatic-hypothalamic gliomas(CHG) include surgery, irradiation, chemotherapy and a combination of these modalities. This study was performed in order to compare the efficacy of various methods of treatment and to describe its optimal management. Material and Method : We have reviewed the results of management of 6 children with a diagnosis of CHG, who were observed closely during the last 8 years. The patients were aged 7 months to 15 years. Our patients presented with diencephalic syndrome, endocrine dysfunction, and progressive visual loss. None of these had evidence of neurofibromatosis-1. Treatment consisted of surgery alone(2), surgry and irradiation(2), surgery, irradiation and chemotherapy(1), and surgery and chemotherapy(1). Results : Four children had large exophytic suprasellar tumors and two showed diffuse midline lesions. Obstructive hydrocephalus was present in all patients. Pathologic examination revealed anaplastic astrocytoma in 1 and lowgrade astrocytoma in 5. Two patients, recently treated with radiation therapy following radical subtotal resection, showed significant tumor reductions and good clinical status. Four patients had partial tumor resection. Of these patients, two developed disease stabilization during follow-up period of 7 and 8 years, respectively. Life-threatening complications were noted in remaining two patients. Conclusion : CHG may follow an unpredicatable course and show a various reponse to each treatment modality. Further studies are indicated to define the optimal method of treatment of CHG in childhood.

Keywords