Cerebral Cavernous Malformations

R. Michael Scott, G. D. Dunn, J. P. Finn, I. F. Moseley, Irvine Mason, John M. Aase, William W. Orrison, Joseph M. Bicknell, Daniele Rigamonti, Mark N. Hadley, Burton P. Drayer, Peter C. Johnson, Karen Hoenig-Rigamonti, J. Thomas Knight, Robert F. Spetzler

Research output: Contribution to journalLetterpeer-review

Abstract

To the Editor: The paper by Rigamonti et al. (Aug. 11 issue)* was timely, since cerebral cavernous malformations are being diagnosed more frequently by magnetic resonance imaging (MRI). The past five vascular malformations in children operated on at the Children's Hospital in Boston this year have been cavernous malformations, all of them symptomatic because of hemorrhage from the lesion associated with neurologic deficit, seizure, or both. We have been advocating the study of family members and siblings when there is a suggestive family history or when the patient has multiple lesions. Rigamonti et al. do not give us any recommendations,.

Original languageEnglish (US)
Pages (from-to)1414-1415
Number of pages2
JournalNew England Journal of Medicine
Volume319
Issue number21
DOIs
StatePublished - Nov 24 1988

ASJC Scopus subject areas

  • Medicine(all)

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