TY - JOUR
T1 - Brain tumors diagnosed in the first year of life in five Far-Eastern countries - Statistical analysis of 307 cases
AU - Oi, S.
AU - Matsumoto, S.
AU - Choi, J. U.
AU - Kang, J. K.
AU - Wong, T.
AU - Wang, C.
AU - Chan, T. S.T.
PY - 1990/3
Y1 - 1990/3
N2 - A statistical survey is presented of brain tumors diagnosed in the first year of life (from five Far-Eastern countries) in relation to the racial differences in tumor types, congenital factors, and general clinical features. Of the 307 cases collected, 262 were verified histologically, and astrocytomas comprised 23.3%, medulloblastomas 17.2%, ependymomas 11.1%, choroid plexus papillomas 10.7%, teratomas 8.4%, primitive neuroectodermal tumors 4.2%, meningiomas 2.3%, and others 22.9%. There were statistically significant racial differences in comparison with the worldwide survey done by the International Society for Pediatric Neurosurgery Education Committee (1987) on the same subject. In the Far-Eastern population, medulloblastoma and teratoma were more common (P<0.05), whereas astrocytoma was less frequent (P<0.01) than reported in the worldwide survey. The malformative factors were suggested in 18 cases in which various associated congential anomalies were observed. Vascular anomalous lesions, mostly in the extracranial organs, were most common, comprising 61.1% of the associated malformations. Hereditary factors were less commonly demonstrated in these tumors than were anomalies in the major congenital central nervous system. Among the 307 cases, there was one instance (0.3%) of nearly identical tumors occurring in twin brothers. The specific clinical manifestations of brain tumors involving the immature brain were again apparent in this survey, as were the poor survival rates and poor functional prognosis.
AB - A statistical survey is presented of brain tumors diagnosed in the first year of life (from five Far-Eastern countries) in relation to the racial differences in tumor types, congenital factors, and general clinical features. Of the 307 cases collected, 262 were verified histologically, and astrocytomas comprised 23.3%, medulloblastomas 17.2%, ependymomas 11.1%, choroid plexus papillomas 10.7%, teratomas 8.4%, primitive neuroectodermal tumors 4.2%, meningiomas 2.3%, and others 22.9%. There were statistically significant racial differences in comparison with the worldwide survey done by the International Society for Pediatric Neurosurgery Education Committee (1987) on the same subject. In the Far-Eastern population, medulloblastoma and teratoma were more common (P<0.05), whereas astrocytoma was less frequent (P<0.01) than reported in the worldwide survey. The malformative factors were suggested in 18 cases in which various associated congential anomalies were observed. Vascular anomalous lesions, mostly in the extracranial organs, were most common, comprising 61.1% of the associated malformations. Hereditary factors were less commonly demonstrated in these tumors than were anomalies in the major congenital central nervous system. Among the 307 cases, there was one instance (0.3%) of nearly identical tumors occurring in twin brothers. The specific clinical manifestations of brain tumors involving the immature brain were again apparent in this survey, as were the poor survival rates and poor functional prognosis.
KW - Brain tumors
KW - Congenital factors
KW - Cooperative survey
KW - Far-Eastern countries
KW - Neonates and infants
KW - Racial differences
UR - https://www.scopus.com/pages/publications/0025374444
UR - https://www.scopus.com/pages/publications/0025374444#tab=citedBy
U2 - 10.1007/BF00307926
DO - 10.1007/BF00307926
M3 - Article
C2 - 2340533
AN - SCOPUS:0025374444
SN - 0256-7040
VL - 6
SP - 79
EP - 85
JO - Child's Nervous System
JF - Child's Nervous System
IS - 2
ER -