Literature DB >> 7472549

The natural history of cerebral cavernous malformations.

D Kondziolka1, L D Lunsford, J R Kestle.   

Abstract

To determine the natural history of brain cavernous malformations, the authors entered patients referred to their center into a prospective registry between 1987 and 1993. All patients underwent magnetic resonance imaging, which showed the typical appearance of this lesion, and conservative management was recommended in all. Patients or their referring physicians were contacted for follow-up data. The purpose of the study was to define the rate of symptomatic hemorrhage and to determine the outcome in those patients who had suffered seizures. Follow-up data were available for 122 patients with a mean age at entry of 37 years (range 4-82 years). The malformation was located in the brainstem in 43 cases (35%), the basal ganglia/thalamus in 20 (17%), and a hemispheric area in 59 (48%). Fifty percent of patients had never had a symptomatic hemorrhage, 41% had one bleed, 7% had two, and 2% had three. Seizures were reported in 23% of patients and headaches in 15%. Lesions were solitary in 80% of patients and multiple in 20%. The retrospective annual hemorrhage rate (61 bleeds/4550.6 patient-years of life) was 1.3%. The mean prospective follow-up period was 34 months. There were nine bleeds during this time, six with new neurological deficits. In patients without a prior bleed, the prospective annual rate of hemorrhage was 0.6%. In contrast, patients with prior hemorrhage had an annual bleed rate of 4.5% (p = 0.028). Patient sex (p = 0.97) or the presence of seizures (p = 0.11), headaches (p = 0.06), or solitary versus multiple lesions (p = 0.15) were not significant predictors of later hemorrhage. There was no difference in the rate of bleeds between brain locations. Four patients with seizures became seizure-free and four patients without seizures later developed seizures; only one patient developed intractable seizures. Fourteen had radiosurgery. No patient died in the follow-up period. This study indicates that conservative versus operative management strategies may need to be redefined, especially in patients who present with hemorrhage and who appear to have a significantly increased risk of subsequent rehemorrhage.

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Year:  1995        PMID: 7472549     DOI: 10.3171/jns.1995.83.5.0820

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


  79 in total

1.  Surgical management of brain-stem cavernomas.

Authors:  U Pechstein; J Zentner; D Van Roost; J Schramm
Journal:  Neurosurg Rev       Date:  1997       Impact factor: 3.042

Review 2.  Management of hemorrhage from cavernous malformations.

Authors:  Sachin Batra; Karen Rigamonti; Daniele Rigamonti
Journal:  Curr Atheroscler Rep       Date:  2012-08       Impact factor: 5.113

Review 3.  Cerebral developmental venous anomalies.

Authors:  Diego San Millán Ruíz; Philippe Gailloud
Journal:  Childs Nerv Syst       Date:  2010-08-12       Impact factor: 1.475

4.  Epilepsy Surgeons, Rather than Vascular Neurosurgeons, Should Operate on Cavernous Malformations that Cause Seizures-A Modest Proposal.

Authors:  Theodore H Schwartz
Journal:  Epilepsy Curr       Date:  2010-05       Impact factor: 7.500

Review 5.  Cystic cavernous angiomas.

Authors:  Shigeo Ohba; Kazuhiko Shimizu; Syunsuke Shibao; Toru Nakagawa; Hideki Murakami
Journal:  Neurosurg Rev       Date:  2010-02-20       Impact factor: 3.042

6.  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

7.  [Recommendations of the European Stroke Initiative for the diagnosis and treatment of spontaneous intracerebral haemorrhage].

Authors:  S Külkens; P Ringleb; J Diedler; W Hacke; T Steiner
Journal:  Nervenarzt       Date:  2006-08       Impact factor: 1.214

8.  Stereotactic LINAC radiosurgery for the treatment of brainstem cavernomas.

Authors:  M Fuetsch; F El Majdoub; M Hoevels; R P Müller; V Sturm; M Maarouf
Journal:  Strahlenther Onkol       Date:  2012-04       Impact factor: 3.621

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.  Two-hit mechanism in cerebral cavernous malformation? A case of monozygotic twins with a CCM1/KRIT1 germline mutation.

Authors:  Philipp Dammann; Ute Hehr; Sabine Weidensee; Yuan Zhu; Rüdiger Gerlach; Ulrich Sure
Journal:  Neurosurg Rev       Date:  2013-04-13       Impact factor: 3.042

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