M. Cerda-nicolas et al., Histopathological and cytogenetic findings in benign, atypical and anaplastic human meningiomas: a study of 60 tumors, CLIN NEUR, 19(6), 2000, pp. 259-267
Meningiomas may display benign (grade I), atypical (grade II) and anaplasti
c (grade III) histopathological findings. The cytogenetic studies strongly
suggest that secondary changes (beyond loss of chromosome 22) appear to be
associated with more atypical features and with greater clinical aggressivi
ty. We studied 60 tumors from 52 patients. Histopathological features such
as nuclear pleomorphism, nucleolar prominence, mitosis, necrosis, cellular
density, PCNA labeling index, and karyotype have been evaluated. The distri
bution in histological grades was: 50% benign, 33% atypical and 17% anaplas
tic meningiomas. Nuclear pleomorphism and nucleolar prominence showed a pro
gressive increase in grades I, II and III. Multifocal micronecrosis was con
sidered a criterion of malignancy. A significant correlation was observed b
etween PCNA-LI, mitotic index and grades. Complex karyotypes increased prog
ressively: benign (34% of cases), atypical (45% of cases) and anaplastic (7
0% of cases). The most common numerical alterations were losses of chromoso
mes 10, 14, 18 and 22. The chromosomes most often involved in structural an
omalies were: 1, 4, 7, 14 and 22. Telomeric associations were present in fo
ur cases and double minutes in two cases. Prognostic criteria for these tum
ors have been analyzed on the basis of these data.