medigraphic.com
SPANISH

Acta Médica Grupo Angeles

Órgano Oficial del Hospital Angeles Health System
  • Contents
  • View Archive
  • Information
    • General Information        
    • Directory
  • Publish
    • Instructions for authors        
    • Send manuscript
    • Names and affiliations of the Editorial Board
  • Policies
  • About us
    • Data sharing policy
    • Stated aims and scope
  • medigraphic.com
    • Home
    • Journals index            
    • Register / Login
  • Mi perfil

2025, Number 4

<< Back Next >>

Acta Med 2025; 23 (4)

Grenet syndrome is caused by slow flow venous malformation (cavernoma) in the pons

Domínguez CLG, Arellano AJG, Hasslacher AJF
Full text How to cite this article 10.35366/120518

DOI

DOI: 10.35366/120518
URL: https://dx.doi.org/10.35366/120518

Language: Spanish
References: 0
Page: 404-405
PDF size: 215.30 Kb.


Key words:

cavermous venous malformation, slow flow venous malformation, cerebral vascular malformation, intracraneal cavernoma.

Cerebral cavernous venous malformations (CVMs) are "slow-flow venous malformations". It is the third most common cerebral vascular malformation, supratentorial in ~80% of cases. Brainstem CVMs are rare (8-22%) of all intracranial cavernomas; 40% are incidental findings. If they occur, their symptoms are between 30 and 60 years of age; they are usually single lesions. The majority remain asymptomatic. Presentation due to bleeding can cause headaches, seizures, and focal neurological deficits. The risk of bleeding is < 0.1 to 1% per patient-year and 5% in the brainstem. Symptomatic lesions should, when possible, be resected, and complete resection is curative.





Figure 1
Figure 2

2020     |     www.medigraphic.com

Mi perfil

C?MO CITAR (Vancouver)

Acta Med. 2025;23