Literature DB >> 1919691

An analysis of the natural history of cavernous angiomas.

O Del Curling1, D L Kelly, A D Elster, T E Craven.   

Abstract

The advent of magnetic resonance (MR) imaging has permitted the recognition of many angiographically occult vascular malformations before the development of complications and subsequent surgical removal. This study reviews all patients at one institution who had radiographically identifiable vascular malformations believed to represent cavernous angiomas in order to obtain information on the natural history of this particular lesion. All 8131 craniospinal MR images performed at our medical center from January 1, 1986, to November 30, 1989, were reviewed, and 32 patients were identified with 76 lesions meeting the MR imaging criteria for cavernous angioma. Medical histories, physical examination records, and other data from these patients were then reviewed to determine the frequency of complications. Their mean age at latest follow-up examination (or at surgical removal of the lesion) was 37.6 years (range 16 to 72 years). Sixteen patients (50%) had a history of seizures, seven (22%) had focal neurological deficits, and three (9%) had clinically significant hemorrhage attributable to the cavernous angioma; six patients (19%) were asymptomatic. The estimated risk of hemorrhage for this population is 0.25%/person-year of exposure; the estimated risk of seizure development is 1.51%/person-year. Eight patients underwent surgical procedures, resulting in improved seizure control and/or lessened neurological deficit. Although these lesions are often excised with relative ease and minimal morbidity, the potential risks and benefits of surgery must be weighed carefully before removal of these relatively benign malformations.

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Mesh:

Year:  1991        PMID: 1919691     DOI: 10.3171/jns.1991.75.5.0702

Source DB:  PubMed          Journal:  J Neurosurg        ISSN: 0022-3085            Impact factor:   5.115


  117 in total

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2.  Familial cavernous malformations in a large French kindred: mapping of the gene to the CCM1 locus on chromosome 7q.

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Review 7.  Cavernous malformations of central nervous system in pediatric patients: our single-centered experience in 50 patients and review of literature.

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Journal:  Childs Nerv Syst       Date:  2017-06-20       Impact factor: 1.475

8.  De novo development of a lesion with the appearance of a cavernous malformation adjacent to an existing developmental venous anomaly.

Authors:  Norbert G Campeau; John I Lane
Journal:  AJNR Am J Neuroradiol       Date:  2005-01       Impact factor: 3.825

9.  Management of intracranial cavernous malformation in pediatric patients.

Authors:  Jae-Whan Lee; Dong-Seok Kim; Kyu-Won Shim; Jong-Hee Chang; Seung-Kon Huh; Yong-Gou Park; Joong-Uhn Choi
Journal:  Childs Nerv Syst       Date:  2007-09-18       Impact factor: 1.475

10.  Prevalence of cerebrovascular diseases that can cause hemorrhagic stroke in liver transplantation recipients: a 6-year comparative study with 24,681 healthy adults.

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Journal:  Neurol Sci       Date:  2020-10-30       Impact factor: 3.307

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