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Cerebral necrosis after radiotherapy and/or intraarterial chemotherapy for brain tumors: PET and neuropathologic studies

American Journal of Roentgenology · 1988 · Vol. 150(1) · pp. 189–197
Giovanni Di ChiroE H OldfieldWright DcD. De MicheleD A KatzN J PatronasJL DoppmanS. M. LarsonMinoru ItoCV Kufta

Abstract

Cerebral necrosis after radiotherapy for brain tumors is being recognized as a problem more common than previously estimated. Distinction between this iatrogenic complication and tumor recurrence cannot be made by either CT or MR imaging. By using positron emission tomography (PET) with 18F-deoxyglucose (FDG) we were able to reach a diagnosis of radiation necrosis, later verified, in 10 of 95 patients referred for the purpose of differentiating tumor recurrence from necrosis. The critical PET-FDG feature was focal hypometabolism in the area of necrosis, which contrasted with the hypermetabolism associated with the residual/recurrent tumor. In addition, four cases of cerebral necrosis after supraophthalmic, intraarterial chemotherapy (BCNU) were studied with the PET-FDG method. The area of chemotherapy damage was also characterized by marked hypometabolism. Histology revealed both similarities and differences between radio- and chemonecrosis.

Diet, Metabolism, and DiseaseElectron Spin Resonance StudiesHeme Oxygenase-1 and Carbon MonoxideMedicineRadiation therapyChemotherapyNecrosisPathologyNuclear medicineRadiologyInternal medicine

MeSH terms

AdolescentAdultAgedBrainBrain NeoplasmsCarmustineChildChild, PreschoolDeoxyglucoseDiagnosis, DifferentialFemaleHumansInfusions, Intra-ArterialMaleMiddle Aged
Citations
425
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8.13
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Radiation response of the central nervous system
International Journal of Radiation Oncology*Biology*Physics · 1995 · 655 citations
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