[Supratentorial primitive neuroectodermal tumor: a single center experience and comparison with the literature]. / Supratentorieller primitiver neuroektodermaler Tumor: Erfahrungen in einem Zentrum im Vergleich zur Literatur.
Klin Padiatr
; 217(3): 153-7, 2005.
Article
en De
| MEDLINE
| ID: mdl-15858707
Supratentorial primitive neuroectodermal tumors (stPNETs) are malignant tumors. We saw within three years six children with stPNETs. In four of the six children radical resection could be achieved. All had craniospinal irradiation and chemotherapy according to the HIT-91 protocol. The two children with incomplete resection died due to tumor progression after 7 and 10 months. Two of the 4 children with complete tumor resection had local relapses 8 months after diagnosis and died after 14 and 18 months. One child had a diffuse meningeal relapse 12 months after diagnosis. Despite (high-dose) systemic chemotherapy and intraventricular mafosfamide, he died 21 months after diagnosis due to tumor although remission could be achieved. Only one child is still in remission 86 months after diagnosis.
Buscar en Google
Colección:
01-internacional
Base de datos:
MEDLINE
Asunto principal:
Lóbulo Parietal
/
Lóbulo Temporal
/
Tálamo
/
Neoplasias Encefálicas
/
Núcleos Cerebelosos
/
Tumores Neuroectodérmicos
/
Cuerpo Calloso
/
Lóbulo Frontal
/
Lóbulo Occipital
Tipo de estudio:
Guideline
/
Prognostic_studies
Límite:
Child
/
Child, preschool
/
Humans
/
Male
Idioma:
De
Revista:
Klin Padiatr
Año:
2005
Tipo del documento:
Article
Pais de publicación:
Alemania