Longitudinal CT study of parenchymal brain changes in glioma survivors

We reviewed the serial CT studies obtained between 1974 and 1986 of 31 patients with malignant glioma who survived for 2 to 11 years after surgical removal of their tumors. In all cases surgery was followed by radiation therapy to the head (6000 rad) and chemotherapy. Patients were divided into two...

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Veröffentlicht in:American journal of neuroradiology : AJNR 1988-05, Vol.9 (3), p.517-522
Hauptverfasser: Stylopoulos, LA, George, AE, de Leon, MJ, Miller, JD, Foo, SH, Hiesiger, E, Wise, A
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container_issue 3
container_start_page 517
container_title American journal of neuroradiology : AJNR
container_volume 9
creator Stylopoulos, LA
George, AE
de Leon, MJ
Miller, JD
Foo, SH
Hiesiger, E
Wise, A
description We reviewed the serial CT studies obtained between 1974 and 1986 of 31 patients with malignant glioma who survived for 2 to 11 years after surgical removal of their tumors. In all cases surgery was followed by radiation therapy to the head (6000 rad) and chemotherapy. Patients were divided into two age groups: those under age 40 (n = 13) and those over age 40 (n = 18). By 2 years all patients in the older group developed evidence of leukoencephalopathy characterized by periventricular zones of decreased attenuation. Only 58% of the younger group showed evidence of white matter changes at this point. All patients from both age groups who survived for 4 years developed leukoencephalopathy. The severity of leukoencephalopathy from 6 months after surgery and beyond was always greater in the older group. All patients developed cerebral atrophy as evidenced by sulcal dilatation and ventricular enlargement. Atrophy was progressive beginning with the first postirradiation scan, and was always more severe in the older patients. A significant difference was found in the clinical status of the two age groups as determined by the mental status score and the Karnofsky scale. Despite progressive brain changes, survivors under age 40 maintained a nearly normal mental status and Karnofsky scores until their death, whereas survivors over age 40 showed progressive clinical decline.
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In all cases surgery was followed by radiation therapy to the head (6000 rad) and chemotherapy. Patients were divided into two age groups: those under age 40 (n = 13) and those over age 40 (n = 18). By 2 years all patients in the older group developed evidence of leukoencephalopathy characterized by periventricular zones of decreased attenuation. Only 58% of the younger group showed evidence of white matter changes at this point. All patients from both age groups who survived for 4 years developed leukoencephalopathy. The severity of leukoencephalopathy from 6 months after surgery and beyond was always greater in the older group. All patients developed cerebral atrophy as evidenced by sulcal dilatation and ventricular enlargement. Atrophy was progressive beginning with the first postirradiation scan, and was always more severe in the older patients. A significant difference was found in the clinical status of the two age groups as determined by the mental status score and the Karnofsky scale. 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In all cases surgery was followed by radiation therapy to the head (6000 rad) and chemotherapy. Patients were divided into two age groups: those under age 40 (n = 13) and those over age 40 (n = 18). By 2 years all patients in the older group developed evidence of leukoencephalopathy characterized by periventricular zones of decreased attenuation. Only 58% of the younger group showed evidence of white matter changes at this point. All patients from both age groups who survived for 4 years developed leukoencephalopathy. The severity of leukoencephalopathy from 6 months after surgery and beyond was always greater in the older group. All patients developed cerebral atrophy as evidenced by sulcal dilatation and ventricular enlargement. Atrophy was progressive beginning with the first postirradiation scan, and was always more severe in the older patients. 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Despite progressive brain changes, survivors under age 40 maintained a nearly normal mental status and Karnofsky scores until their death, whereas survivors over age 40 showed progressive clinical decline.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Brain - pathology</subject><subject>Brain - radiation effects</subject><subject>Brain Damage, Chronic - pathology</subject><subject>Brain Neoplasms - radiotherapy</subject><subject>Brain Neoplasms - surgery</subject><subject>Carmustine - administration &amp; dosage</subject><subject>Combined Modality Therapy</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Glioma - radiotherapy</subject><subject>Glioma - surgery</subject><subject>Humans</subject><subject>Leukoencephalopathy, Progressive Multifocal - pathology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Neurology</subject><subject>Postoperative Complications - pathology</subject><subject>Radiation Injuries - pathology</subject><subject>Research Support, U.S. Gov't, P.H.S</subject><subject>Tomography, X-Ray Computed</subject><subject>Tumors of the nervous system. 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Phacomatoses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stylopoulos, LA</creatorcontrib><creatorcontrib>George, AE</creatorcontrib><creatorcontrib>de Leon, MJ</creatorcontrib><creatorcontrib>Miller, JD</creatorcontrib><creatorcontrib>Foo, SH</creatorcontrib><creatorcontrib>Hiesiger, E</creatorcontrib><creatorcontrib>Wise, A</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>American journal of neuroradiology : AJNR</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stylopoulos, LA</au><au>George, AE</au><au>de Leon, MJ</au><au>Miller, JD</au><au>Foo, SH</au><au>Hiesiger, E</au><au>Wise, A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Longitudinal CT study of parenchymal brain changes in glioma survivors</atitle><jtitle>American journal of neuroradiology : AJNR</jtitle><addtitle>AJNR Am J Neuroradiol</addtitle><date>1988-05-01</date><risdate>1988</risdate><volume>9</volume><issue>3</issue><spage>517</spage><epage>522</epage><pages>517-522</pages><issn>0195-6108</issn><eissn>1936-959X</eissn><coden>AAJNDL</coden><abstract>We reviewed the serial CT studies obtained between 1974 and 1986 of 31 patients with malignant glioma who survived for 2 to 11 years after surgical removal of their tumors. 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subjects Adolescent
Adult
Aged
Antineoplastic Combined Chemotherapy Protocols - therapeutic use
Biological and medical sciences
Brain - pathology
Brain - radiation effects
Brain Damage, Chronic - pathology
Brain Neoplasms - radiotherapy
Brain Neoplasms - surgery
Carmustine - administration & dosage
Combined Modality Therapy
Female
Follow-Up Studies
Glioma - radiotherapy
Glioma - surgery
Humans
Leukoencephalopathy, Progressive Multifocal - pathology
Male
Medical sciences
Middle Aged
Neurology
Postoperative Complications - pathology
Radiation Injuries - pathology
Research Support, U.S. Gov't, P.H.S
Tomography, X-Ray Computed
Tumors of the nervous system. Phacomatoses
title Longitudinal CT study of parenchymal brain changes in glioma survivors
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