I. Salmon et al., STEREOTAXIC BIOPSIES FROM ASTROCYTIC TUMORS - DIAGNOSTIC INFORMATION CONTRIBUTED BY THE QUANTITATIVE CHROMATIN PATTERN DESCRIPTION, Analytical and quantitative cytology and histology, 17(5), 1995, pp. 332-343
OBJECTIVE: To reduce the problem of heterogeneity in astrocytic tumors
by means of computer-assisted microscope analysis of Feulgen-stained
nuclei. STUDY DESIGN: Thirty-eight glial tumors for which we obtained
227 stereotactic biopsies were subjected to digital cell image analysi
s of Feulgen-stained nuclei. This series of 38 glial tumors included 3
6 supratentorial astrocytic tumors (13 astrocytomas, 7 anaplastic astr
ocytomas and 16 glioblastoma multiformes) and 2 grade 3 astrocytic tum
ors of the cerebellum. RESULTS: The results suggest a new methodology,
enabling the biologic characteristics of the brain parenchymal area s
urrounding a given glial tumor to be characterized. This methodology r
elies on the performance of three successive steps. The first is quant
itative characterization of nuclear morphology and its chromatin patte
rn by means of 15 morphonuclear variables. This characterization is ca
rried out by means of the computer-assisted microscope analysis of Feu
lgen-stained nuclei. The second step consists of setting up morphonucl
ear data banks, with each process giving the precise portrait of a giv
en cell nuclear population. This process is carried out by means of mu
ltivariate analysis, taking into account the 15 variables mentioned ab
ove. Multivariate analysis includes principal components analysis foll
owed by the canonical transformation of the data. The third step consi
sts of testing unknown cases against these morphonuclear data banks. T
his is carried out by means of linear discriminant analysis, which ena
bles the various cell nuclear types in the stereotactic biopsy to be q
uantified. CONCLUSION: The present methodology makes if possible to in
vestigate whether infiltrating tumor cells are present in or absent fr
om the parenchymal brain area surrounding a glial tumor. It can theref
ore contribute additional information to that contributed by computed
tomography and/or magnetic resonance imaging with respect to the preci
se delineation of the volume of a brain tumor. This delineation must b
e as precise as possible to allow total surgical resection of the tumo
r and prevention of its recurrence.