Skip Navigation

Neuro-Oncology 1999 1(4):275-281; doi:10.1093/neuonc/1.4.275
© 1999 by Society
This Article
Right arrow Abstract Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrowScopus Links
Google Scholar
Right arrow Articles by De Winter, A. E.
Right arrow Articles by Copeland, D. R.
Right arrow Search for Related Content
PubMed
Right arrow Articles by De Winter, A. E.
Right arrow Articles by Copeland, D. R.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© 1999 by the Society forNeuro-Oncology

Brain tumors in children with neurofibromatosis: Additionalneuropsychological morbidity?

Anne E. De Winter, Bartlett D. Moore, III2, John M. Slopis, Joann L. Ater and Donna R. Copeland

The University of Texas, M.D. Anderson Cancer Center,Houston, TX 77030 (A.E.D., B.D.M., J.M.S., J.L.A., D.R.C.); and The University of Texas-Houston, Medical School, Houston,TX 77030 (J.M.S.)

2 Address correspondence and reprint requests to Bartlett D. Moore, III, Ph.D.,Division of Pediatrics, Box 87, U.T. M.D. Anderson Cancer Center, 1515Holcombe Blvd., Houston, TX 77030.

Neurofibromatosis type 1 is a common autosomal dominant genetic disorderassociated with numerous physical anomalies and an increased incidence ofneuropsychological impairment. Tumors of the CNS occur in approximately 15% ofchildren with neurofibromatosis, presenting additional risk for cognitiveimpairment. This study examines the impact of an additional diagnosis of braintumor on the cognitive profile of children with neurofibromatosis. Acomprehensive battery of neuropsychological tests was administered to 149children with neurofibromatosis. Thirty-six of these children had acodiagnosis of brain tumor. A subset of 36 children with neurofibromatosisalone was matched with the group of children diagnosed with neurofibromatosisand brain tumor. Although mean scores of the neurofibromatosis plus braintumor group were, in general, lower than those of the neurofibromatosis alonegroup, these differences were not statistically significant. Children in theneurofibromatosis plus brain tumor group who received cranial irradiation(n = 9) demonstrated weaker academic abilities than did children withbrain tumor who had not received that treatment. These results suggest thatneurofibromatosis is associated with impairments in cognitive functioning, butthe severity of the problems is not significantly exacerbated by thecodiagnosis of a brain tumor unless treatment includes cranialirradiation.

Received January 15, 1999; Accepted May 17, 1999



References

    Beery, K., and Butenika, N. (1967)Developmental Test of Visual-Motor Integration.Chicago, Ill.: Follett Education Co.

    Brookshire, B., Copeland, D.R., Moore, B.D., and Ater, J.L.(1990) Pretreatment neuropsychological status and associatedfactors in children with primary brain tumors.Neurosurgery 27,887-891.[CrossRef][Web of Science][Medline]

    Buschke, H., and Fuld, P.A. (1974) Evaluating storage,retention, and retrieval in disordered memory and learning.Neurology 24,1019-1025.[Abstract/Free Full Text]

    Cohen, B.H., Kaplan, A.M., and Packer, R.J.(1990–91) Management of intracranial neoplasms in childrenwith neurofibromatosis type 1 and 2. Pediatr.Neurosurg. 16,66-72.

    Cohen, M.E., Duffner, P.K., Kuhn, J.P., and Seidel, F.G.(1986) Neuroimaging in neurofibromatosis. Ann.Neurol. 20,444.

    Copeland, D.R., and Moore, B.D. (1992)Neuropsychological outcome among children treated at M.D. Anderson CancerCenter. Can. Bull. 44,509-517.

    Copeland, D.R., Fletcher, J.M., Pfefferbaum-Levine, B., Jaffe, N.,Ried, H., and Maor, M. (1985) Neuropsychological sequelae ofchildhood cancer in long-term survivors. Pediatrics75,745-753.[Abstract/Free Full Text]

    Copeland, D.R., Dowell, R.E., Jr., Fletcher, J.M., Bordeaux, J.D.,Sullivan, M.P., Jaffe, N., Frankel, L.S., Ried, H.L., and Cangir, A.(1988) Neuropsychological effects of childhood cancer treatment.J. Child. Neurol. 3,53-62.[Abstract/Free Full Text]

    Crossen, J.R., Garwood, D., Glatstein, E., and Neuwelt, E.A.(1994) Neurobehavioral sequelae of cranial irradiation in adults:A review of radiation-induced encephalopathy. J. Clin.Oncol. 12,627-642.[Abstract]

    Denckla, M.B., and Rudel, R. (1974) Rapid"automatized" naming of pictured objects, colors, letters, andnumbers by normal children. Cortex10,186-202.[Medline]

    Denckla, M.B., Hofman, K., Mazzocco, M.M., Melhem, E., Reiss, A.L.,Bryan, R.N., Harris, E.L., Lee, J., Cox, C.S., and Schuerholz, L.J.(1996) Relationship between T2-weighted hyperintensities(unidentified bright objects) and lower IQs in children withneurofibromatosis-1. Am. J. Med. Genet.67, 98-102.[CrossRef][Web of Science][Medline]

    Duffner, P.K., Cohen, M.E., Seidel, F.G., and Shucard, D.W.(1989) The significance of MRI abnormalities in children withneurofibromatosis. Neurology39,373-378.[Abstract/Free Full Text]

    Eldridge, R., Denckla, M.B., Bien, E., Myers, S., Kaiser-Kupfer,M.I., Pikus, A., Schlesinger, S.L., Parry, D.M., Dambrosia, J.M., Zasloff,M.A., Mulvihill, J.J. (1989) Neurofibromatosis type 1(Recklinghausen's disease): Neurologic and cognitive assessment with siblingcontrols. Am. J. Dis. Child.143,833-837.[Abstract/Free Full Text]

    Eliason, M.J. (1986) Neurofibromatosis: Implicationsfor learning and behavior. J. Dev. Behav. Pediatr.7, 175-179.[Web of Science][Medline]

    Ferner, R.E., Chaudhuri, R., Bingham, J., Cos, T., and Hughes,R.A.C. (1993) MRI in neurofibromatosis 1: The nature andevolution of increased intensity T2 weighted lesions and their relationship tointellectual impairment. J. Neurol. Neurosurg.Psychiatry 56,492-495.[Abstract/Free Full Text]

    Fletcher, J.M. (1985) Memory for verbal and nonverbalstimuli in learning disabled subgroups: Analysis by selective reminding.J. Exp. Child Psychol.40,244-259.[CrossRef][Web of Science][Medline]

    Fletcher, J.M., and Copeland, D.R. (1988)Neurobehavioral effects of central nervous system prophylactic treatment ofcancer in children. J. Clin. Exp. Neuropsychol.10,495-537.[Web of Science][Medline]

    Gaddes, W.H., and Crockett, D.J. (1975) TheSpreen-Benton aphasia tests: Normative data as a measure of normal languagedevelopment. Brain Lang.2, 257-280.[CrossRef][Web of Science][Medline]

    Hofman, K.J., Harris, E.L., Bryan, R.N., and Denckla, M.B.(1994) Neurofibromatosis type 1: The cognitive phenotype.J. Pediatr. 124,S1-S8.[CrossRef][Web of Science][Medline]

    Hollingshead, A.B. (1975) Four Factor Indexof Social Status. New Haven, Conn.: Yale University.

    Jastak, S.R., and Wilkinson, G.S. (1984)WRAT-R: Wide Range Achievement Test-Revised AdministrationManual. Wilmington, Del.: Jastak Associates, Inc.

    Joy, P., Roberts, C., North, K., and de Silva, M.(1995) Neuropsychological function and MRI abnormalities inneurofibromatosis type I. Dev. Med. Child Neurol.37,906-914.[Web of Science][Medline]

    Legius, E., Descheemaeker, M.J., Spaepen, A., Casaer, P., andFryns, J.P. (1994) Neurofibromatosis type 1 in childhood: A studyof the neuropsychological profile in 45 children. Genet.Counseling 5,51-60.

    Leiner, H.C., Leiner, A.L., and Dow, R.S. (1991) Thehuman cerebro-cerebellar system: Its computing, cognitive, and languageskills. Behav. Brain Res.44,113-128.[Web of Science][Medline]

    Lindgren, S.D., and Benton, A.L. (1980) Developmentalpatterns of visuospatial judgment. J. Pediatr.Psychol. 5,217-225.

    Listernick, R., Charrow, J., Greenwald, M.J., and Easterly, N.B.(1989) Optic gliomas in children with neurofibromatosis type 1.J. Pediatr. 114,788-792.[CrossRef][Medline]

    Listernick, R., Charrow, J., and Greenwald, M. (1992)Emergence of optic pathway gliomas in children with neurofibromatosis type 1after normal neuroimaging results. J. Pediatr.121,584-587.[CrossRef][Web of Science][Medline]

    Listernick, R., Charrow, J., Greenwald, M., and Mets, M.(1994) Natural history of optic pathway tumors in children withneurofibromatosis type 1: A longitudinal study. J.Pediatr. 125,63-66.[CrossRef][Web of Science][Medline]

    Mazzocco, M.M., Turner, J.E., Denckla, M.B., Hofman, K.J., Scanlon,D.C., and Vellutino, F.R. (1997) Language and reading deficitsassociated with neurofibromatosis type 1: Evidence for a not-so-nonverballearning disability. Dev. Neuropsychol.11,504-522.

    McCarthy, D. (1972) McCarthy Scales ofChildren's Abilities. New York, N.Y.: The PsychologicalCorporation.

    Moore, B.D., III, Ater, J.L., Needle, M.N., Slopis, J., andCopeland, D.R. (1994) Neuropsychological profile of children withneurofibromatosis, brain tumor, or both. J. ChildNeurol. 9,368-377.

    Moore, B.D., Slopis, J.M., Schomer, D., Jackson, E.F., and Levy,B.M. (1996) Neuropsychological significance of areas of highsignal intensity on brain MRIs of children with neurofibromatosis.Neurology 46,1660-1668.[Abstract/Free Full Text]

    Mulvihill, J.J., Parry, D.M., Sherman, J.L., Pikus, A.,Kaiser-Kupfer, M.I., and Eldridge, R. (1990) NIH conference.Neurofibromatosis 1 (Recklinghausen disease) and neurofibromatosis 2(bilateral acoustic neurofibromatosis): An update. Ann. InternalMed. 113,39-52.

    NIH (National Institutes of Health) (1988)Neurofibromatosis conference statement. National Institutes of Healthconsensus Development Conference. Arch. Neurol.45,575-578.[Abstract/Free Full Text]

    North, K., Joy, P., Yuille, D., Cocks, N., Mobbs, E., Hutchins, P.,McHugh, K., and de Silva, M. (1994) Specific learning disabilityin children with neurofibromatosis type 1: Significance of MRI abnormalities.Neurology 44,878-883.[Abstract/Free Full Text]

    North, K.N., Riccardi, V., Samango-Sprouse, C., Ferner, R., Moore,B., Legius, E., Ratner, N., and Denckla, M.B. (1997) Cognitivefunction and academic performance in neurofibromatosis 1: Consensus statementfrom the NF1 Cognitive Disorders Task Force. Neurology48,1121-1127.[Free Full Text]

    Packer, R.J., Meadows, A.T., Rorke, L.B., Goldwein, J.L., andD'Angio, G. (1987) Long-term sequelae of cancer treatment on thecentral nervous system in childhood. Med. Pediatr.Oncol. 15,241-253.

    Reitan, R. (1969) Manual for Administrationof Neuropsychological Test Batteries on Adults and Children.Bloomington, Ind.: Indiana University Press.

    Riccardi, V.M. (1981) Von Recklinghausenneurofibromatosis. N. Engl. J. Med.305,1617-1627.[Web of Science][Medline]

    Riccardi, V.M. (1982) The multiple forms ofneurofibromatosis. Pediatr. Rev.3, 293-298.[Abstract/Free Full Text]

    Ris, M.D., and Noll, R.B. (1994) Long-termneurobehavioral outcome in pediatric brain-tumor patients: Review andmethodological critique. J. Clin. Exp. Neuropsychol.16, 21-42.[Web of Science][Medline]

    Roos, K.L., and Dunn, D.W. (1992) Neurofibromatoses.CA Cancer J. Clin. 42,241-254.[Web of Science][Medline]

    Rosner, J., and Simon, D.P. (1971) The AuditoryAnalysis Test: An initial report. J. Learn. Dis.7, 40-47.

    Satz, P., and Fletcher, J.M. (1982) TheFlorida Kindergarten Screening Battery. Odessa, Fla.:Psychological Assessment Resources, Inc.

    Stine, S.B., and Adams, W.V. (1989) Learning problemsin neurofibromatosis patients. Clin. Orthop.245, 43-48.[Medline]

    Thorndike, R.L., Hagen, E.P., and Sattler, J.M. (1986)Stanford-Binet Intelligence Scale: Guide for Administering andScoring the Fourth Edition. Fourth edition. Chicago: TheRiverside Publishing Company.

    Varnhagen, C.K., Lewin, S., Das, J.P., Bowen, P., Ma, K., andKlimek, M. (1988) Neurofibromatosis and psychological processes.J. Dev. Behav. Pediatr.9, 257-265.[Web of Science][Medline]

    Wadsby, M., Lindehammar, H., and Eeg-Olofsson, O.(1989) Neurofibromatosis in childhood: Neuropsychologicalaspects. Neurofibromatosis2, 251-260.[Medline]

    Wechsler, D. (1974) WISC-R, Manual for theWechsler Intelligence Scale for Children-Revised. New York, N.Y.:The Psychological Corporation.

    Wechsler, D. (1991) Wechsler IntelligenceScale for Children. Third edition. New York, N.Y.: Harcourt,Brace, Jovancovich, Inc.,

    Woodcock, R.W., Johnson, M.B., and Mather, N. (1989)Woodcock Johnson Psycho-Educational Battery-Revised.Allen, Texas: DLM Teaching Resources.

    Wright, T.L., and Bresnan, M.J. (1976)Radiation-induced cerebrovascular disease in children.Neurology 26,540-543.[Abstract/Free Full Text]


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Arch NeurolHome page
R. L. Billingsley, G. W. Schrimsher, E. F. Jackson, J. M. Slopis, and B. D. Moore III
Significance of Planum Temporale and Planum Parietale Morphologic Features in Neurofibromatosis Type 1
Arch Neurol, April 1, 2002; 59(4): 616 - 622.
[Abstract] [Full Text] [PDF]


This Article
Right arrow Abstract Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrowScopus Links
Google Scholar
Right arrow Articles by De Winter, A. E.
Right arrow Articles by Copeland, D. R.
Right arrow Search for Related Content
PubMed
Right arrow Articles by De Winter, A. E.
Right arrow Articles by Copeland, D. R.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?