Mb. Bhattacharjee et al., CYTOGENETIC ANALYSIS OF 120 PRIMARY PEDIATRIC BRAIN-TUMORS AND LITERATURE-REVIEW, Cancer genetics and cytogenetics, 97(1), 1997, pp. 39-53
We report chromosome results from 108 pediatric central nervous system
(CNS) tumors. From our data and those in the literature we found that
(1) cerebellar and low-grade astrocytic tumors, including ganglioglio
mas, are most often karyotypically normal; (2) supratentorial tumors w
ere more frequently high-grade tumors that demonstrated a complex kary
otype. Chromosome abnormalities were similar to those described in adu
lt astrocytic tumors, namely, +7, 9p abnormalities, and -10; (3) primi
tive neuroectodermal rumors (PNETs) were virtually always karyotypical
ly abnormal with a high frequency of +7, -8, i(17q), and -22. PNETs wi
th -22 may represent a subset of tumors; (4) typical choroid plexus pa
pillomas showed a normal karyotype, atypical papillomas showed a hyper
diploid karyotype (with +7, +12, and +20), choroid plexus carcinomas s
howed a hyperhaploid karyotype; (5) a few ependymomas showed hyperdipl
oidy or hypertetraploidy; (6) germ cell tumors showed complicated kary
otypes; (7) monosomy 22 or 22q abnormalities appear to be a recurring
finding in the malignant rhabdoid tumors; and (8) meningiomas showed -
22 or 22q abnormalities associated with a complex karyotype. In genera
l, in pediatric CNS tumors the least differentiated neoplasms have the
greatest number of cytogenetic abnormalities. However, our present mo
rphologic criteria for tumor diagnosis do not always correlate with a
consistent karyotype, and further study of pediatric brain tumor morph
ology, site, behavior, and karyotype is required. (C) 1997 Elsevier Sc
ience Inc., 1997.