Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

[Cerebral cavernomas--clinical aspects and therapy]

J Meixensberger1, E Hofmann, K Roosen

  • 1Abteilung für Neuroradiologie, Universität Würzburg, Deutschland.

Wiener Medizinische Wochenschrift (1946)
|January 1, 1997
PubMed
Summary

Cavernomas, or congenital cerebrovascular hamartomas, are vascular malformations affecting 0.4-0.5% of the population. Treatment involves microsurgical resection for symptomatic cases, with careful consideration for deep-seated lesions.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Management of Invasive Pulmonary Aspergillosis in Intensive Care Units: Guidelines From the Fungal Infection Network of Switzerland (FUNGINOS).

Mycoses·2025
Same author

The Use of Shape Memory Alloys in Cages for Cervical Spinal Surgery.

Journal of neurological surgery. Part A, Central European neurosurgery·2025
Same author

Time Trends in Causes of Death in People With HIV: Insights From the Swiss HIV Cohort Study.

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America·2024
Same author

[Erratum to: Interdisciplinary neurovascular networks: state of the art].

Der Nervenarzt·2020
Same author

[Interdisciplinary neurovascular networks: state of the art].

Der Nervenarzt·2020
Same author

Endoscopic resection of an intraventricular cavernoma: a case report.

International medical case reports journal·2019

Area of Science:

  • Neurology
  • Vascular Malformations
  • Neurosurgery

Context:

  • Cavernomas are congenital cerebrovascular hamartomas.
  • They are characterized by sinusoidal blood-filled spaces without distinct arterial feeders or draining veins.
  • These lesions occur sporadically or familially throughout the central nervous system.

Purpose:

  • To describe the epidemiology, clinical presentation, natural course, and management of cavernomas.
  • To evaluate the risks associated with natural progression versus surgical intervention.
  • To outline treatment strategies including microsurgical resection and radiosurgery.

Summary:

  • Cavernomas affect 0.4-0.5% of the population, presenting with hemorrhage, seizures, or focal deficits, though 20% are asymptomatic.

Related Experiment Videos

  • The annual risk of bleeding is 0.6%, and epilepsy risk is 1.5%.
  • Microsurgical resection is the primary treatment for symptomatic superficial cavernomas with low morbidity; deep-seated lesions require careful risk-benefit assessment.

    • Impact:

    • Informs clinical decision-making for cavernoma management, balancing surgical risks with natural progression.
    • Highlights the importance of individualized treatment approaches based on lesion location and patient symptoms.
    • Contributes to understanding the natural history and potential complications of cavernomas.