Topographic anatomy and CT correlations in the untreated glioblastoma multiforme
- PMID: 2833587
- DOI: 10.3171/jns.1988.68.5.0698
Topographic anatomy and CT correlations in the untreated glioblastoma multiforme
Abstract
To provide baseline information for the "local" therapy of the glioblastoma multiforme (GBM), whole-brain histological sections of 15 untreated GBM's were studied to determine the distribution of neoplastic cells. These findings were then compared with the computerized tomography (CT) scans in 11 cases in order to determine the extent to which the peripheral portion of the neoplasm can be estimated by the presence of a low-density area without contrast enhancement. The results of the histological study confirmed the marked heterogeneity of GBM's and disclosed a great variability in the geometry, extent, and character of the peripheral "infiltrating" margin. In spite of the widely held concept that glioblastomas are localized within 2 cm of the contrast-enhanced rim, there were three cases in this two-dimensional study in which this distance was exceeded, and it seems likely that three-dimensional reconstructions would have detected additional cases in which neoplastic cells extended beyond this arbitrary limit. Only three of the 15 GBM's were restricted to the distribution of one internal carotid or one vertebral artery. To the extent that the neoplasms in the present series are representative, this suggests that glioblastomas will be difficult to treat successfully by intra-arterial therapy using existing therapeutic agents. Correlations of histological sections with the CT scans revealed that the vast majority of the neoplastic tissue was contained within the contrast-enhancing and "peritumoral" areas of low density, but that in five cases fingers of neoplasm extended for short distances beyond the outer margin of the latter region. This indicates that the distribution of cells of a GBM cannot be inferred from CT images since the "peritumoral" area of low density can over- or underestimate the extent of the lesion.
Similar articles
-
Computerized tomographic and pathologic studies of the untreated, quiescent, and recurrent glioblastoma multiforme.J Neurosurg. 1983 Feb;58(2):159-69. doi: 10.3171/jns.1983.58.2.0159. J Neurosurg. 1983. PMID: 6294260
-
Pathologic anatomy and CT correlations in the glioblastoma multiforme.Appl Neurophysiol. 1983;46(1-4):180-7. Appl Neurophysiol. 1983. PMID: 6322685
-
Radiation therapy treatment planning in supratentorial glioblastoma multiforme: an analysis based on post mortem topographic anatomy with CT correlations.Int J Radiat Oncol Biol Phys. 1989 Dec;17(6):1347-50. doi: 10.1016/0360-3016(89)90548-8. Int J Radiat Oncol Biol Phys. 1989. PMID: 2557310
-
Pathologic analysis of primary brain tumors.Neurol Clin. 1985 Nov;3(4):711-28. Neurol Clin. 1985. PMID: 3001488 Review.
-
[Autopsy cases of glioblastoma multiforme: treatment results of high-dose fractionated radiation therapy and CT scan findings].Gan No Rinsho. 1989 Sep;35(11):1339-46. Gan No Rinsho. 1989. PMID: 2554007 Japanese.
Cited by
-
Phase II evaluation of high-dose intravenous cisplatin for treatment of adult malignant gliomas recurrent after chloroethylnitrosourea failure.J Neurooncol. 1992 Feb;12(2):187-91. doi: 10.1007/BF00172671. J Neurooncol. 1992. PMID: 1560266 Clinical Trial.
-
Volumetric and MGMT parameters in glioblastoma patients: survival analysis.BMC Cancer. 2012 Jan 3;12:3. doi: 10.1186/1471-2407-12-3. BMC Cancer. 2012. PMID: 22214427 Free PMC article.
-
A phase II pilot randomized controlled trial to assess the feasibility of the "supra-marginal" surgical resection of malignant glioma (G-SUMIT: Glioma supra marginal incision trial) study protocol.Pilot Feasibility Stud. 2022 Jul 5;8(1):138. doi: 10.1186/s40814-022-01104-1. Pilot Feasibility Stud. 2022. PMID: 35791008 Free PMC article.
-
Dynamics of C6 astrocytoma invasion into three-dimensional collagen gels.J Neurooncol. 2001 Jun;53(2):87-98. doi: 10.1023/a:1012236830230. J Neurooncol. 2001. PMID: 11716073
-
Angiogenesis, metastasis, and endogenous inhibition.J Neurooncol. 2000 Oct-Nov;50(1-2):173-80. doi: 10.1023/a:1006453428013. J Neurooncol. 2000. PMID: 11245277 Review.
Publication types
MeSH terms
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical