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Gefäßerkrankungen

Kavernom (zerebrale kavernöse Malformation)

Ein Kavernom ist eine Gefäßmalformation des Gehirns oder Rückenmarks aus dünnwandigen, erweiterten Gefäßräumen, die Blutungen oder Anfälle verursachen kann.

Zuletzt aktualisiert: 2026-06-06

Definition

A cerebral cavernous malformation (cavernoma) is a lesion composed of dilated, thin-walled capillary-like spaces with no intervening normal brain tissue. On imaging it is often described as having a 'mulberry' or 'popcorn' appearance. It may be single (sporadic) or familial and multifocal.

Causes and Risk Factors

Lesions may be sporadic or hereditary (autosomal dominant; associated with the CCM1/KRIT1, CCM2 and CCM3 genes). The familial form tends to produce multiple lesions. Some cavernomas may develop after previous brain radiotherapy.

Symptoms

Many cavernomas are asymptomatic and found incidentally. When symptomatic, the most common features are seizures, lesional hemorrhage and focal neurological signs (weakness, sensory loss, balance problems) depending on location. Brainstem cavernomas can cause prominent symptoms even with small bleeds.

Diagnosis

Magnetic resonance imaging (MRI) is the key modality; gradient-echo and SWI sequences in particular sensitively reveal small lesions and traces of prior hemorrhage. Because cavernomas are low-flow, they are usually not visible on conventional catheter angiography ('angiographically occult').

Treatment

For asymptomatic cavernomas, imaging surveillance is often preferred. For recurrent hemorrhage, drug-resistant seizures or progressive deficit, microsurgical removal is considered for accessible lesions. In high-risk areas such as the brainstem, the decision is individualized by balancing bleeding risk against surgical risk.

Prognosis

Many cavernomas remain silent; bleeding risk varies with lesion location, prior hemorrhage and the familial form. In appropriately selected surgical cases, complete removal reduces the risk of rebleeding. Outcomes vary from patient to patient and are not guaranteed.

Quellen

  1. Akers A, et al. Synopsis of Guidelines for the Clinical Management of Cerebral Cavernous Malformations. Neurosurgery. 2017.
  2. Flemming KD, et al. Cavernous Malformations: Natural History and Management. Mayo Clin Proc.
  3. StatPearls — Cerebral Cavernous Malformations. NCBI Bookshelf.
Autor / Redakteur
Doç. Dr. Özgür Akşan
Beyin ve Sinir Cerrahisi Uzmanı
19 yıllık uzmanlık deneyimi

Dieser Artikel dient der allgemeinen Information und ersetzt keine ärztliche Untersuchung. Diagnose und Behandlung sind individuell.