Cavernous Malformation (Cavernoma):


Contents of This Section:

What is a cavernous malformation (cavernoma)?
How common is a cavernous malformation (cavernoma)?
Why does a cavernous malformation (cavernoma) develop?
What are the symptoms of a cavernous malformation (cavernoma)?
More about cavernous malformation (cavernoma) hemorrhage and rehemorrhage.
What are the complications of a cavernous malformation (cavernoma)?
How is a cavernous malformation (cavernoma) detected?
How is a cavernous malformation (cavernoma) treated?
Images of a cavernous malformation (cavernoma).

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1. What is a cavernous malformation (cavernoma)?

A cavernous malformation, also known as a cavernous hemangioma or cavernoma, is an abnormal vascular entity (or "lesion") made up of many small compartments (lobules) like a bunch of small berries, or a mulberry (see section 9., below, for an image). These microcomparments contain blood (hemorrhagic) products in different stages of evolution. The "sinusoidal" compartments are enclosed by abnormally thin and quite fragile endothelialized walls. Unlike an arteriovenous malformation (AVM; take me to the AVM section now), there is no large feeding artery and no large draining vein in a cavernoma. However, there frequently is a venous angioma associated with the cavernoma! ( take me to the Venous Angioma section now ).

Most cavernomas are found in the larger (supratentorial) parts of the brain hemispheres, but up to 1 in 4 or 5 are found in the hindbrain (posterior fossa; infratentorial), especially in the pons region of the brainstem. Much less commonly a cavernoma may be found in the spinal cord (but this may be more likely to occur in patients with a family history of cavernous malformations).

2. How common are cavernous malformations (cavernomas)?

They are not very common. Their prevalence (presence at any given time) in the population is probably somewhere between 0.1 - 0.5%; they are about as common as brain arteriovenous malformations (AVM), and far less common than brain aneurysms.

3. Why do cavernous malformations (cavernomas) develop?

Cavernomas occur sporadically (spontaneously in a noninherited manner) in the majority of cases, but in some cases may demonstrate inheritance (familial; i.e., a positive or strong family history of cavernous malformations). In familial cases, a specific chromosome 7 gene abnormality has been demonstrated, and familial cavernous malformation has been reported to be more common in hispanic (especially Mexican-American) persons. In familial cases, cavernous malformations are more commonly multiple (i.e., two or more cavernomas present at the time of diagnosis), and may certainly also involve the spinal cord.

On chromosome 7, the specific two genes involved are refered to as CCM1 (band 7q11.2-q21; aka KRIT 1 because of its role in creating the KRIT 1 protein, or Krev interaction-trapped 1 protein), and CCM 2 (band 7p15-p13; controls production of the protein malcavernin). A third gene referred to as CCM 3 (on chromosome 3q) has been identified and is being investigated further.

4. What are the symptoms of cavernous malformations (cavernomas)?

Cavernomas may be asymptomatic, or may present with seizures (60%) or with progressive neurological impairment or "deficits" (50%). Some can present with hydrocephalus or raised intracranial pressure (headache, nausea, vomiting, visual disturbance, sleepiness) depending on their size and location. It is uncommon for cavernomas to cause sudden catastrophic or devastating neurological injury, but the progressive brain (or spinal cord) injury associated with cavernomas may be severely disabling as time goes on.

Why do these symptoms occur? The reason is repeated bouts of hemorrhage in the cavernoma. Different cavities of the cavernoma may have different ages of blood products. The walls are fragile, and the growth of micro blood vessels into these lesions results in blood product (hemosiderin) leeching around the cavernoma, and cycles of cavernoma growth through hemorrhage and rehemorrhage. The hemorrhage is rarely a large devastating hemorrhage.

5. More about cavernous malformation (cavernoma) hemorrhage and rehemorrhage.

The risk of hemorrhage from a cavernoma is somewhere between 0.5-1% per year. It may be greater (or at least easier felt symptomatically) in cavernomas located in more "eloquent" brain such as the basal ganglia, thalamus, brainstem, and spinal cord. The rehemorrhage rate varies in the literature, but is probably somewhere between 4-10% per year (some reports indicate an even higher rate in the first year or two following the first diagnosed cavernoma hemorrhage).

6. What are the complications of cavernous malformations (cavernomas)?

The major complications are seizures and progressive neurological impairment, and the type of "deficit" varies according to the size and location of the cavernoma, and the extent and multiplicity of the hemorrhage(s).

7. How are cavernous malformations (cavernomas) detected?

Cavernomas are detected best through MRI. They can enhance with contrast, but frequently do not. They are not detectable on a cerebral angiogram (i.e., are referred to as angiographically occult vascular malformations or AOVMs; however, an associated venous angioma may be detected on the angiogram!). The best two MRI sequences used to detect cavernomas are regular T2 ("popcorn" appearance) and gradient echo (GRE; "India ink" blotch appearance). These are shown below. A CAT scan can also show a cavernoma, but the resolution is better with an MRI.

Note that in familial or multiple cavernoma patients, it is worthwhile screening the cervicothoracic spinal cord via MRI to exclude the presence of an occult cavernoma there.

8. How are cavernous malformations (cavernomas) treated?

The treatment is surgery. There is no effective radiation treatment for cavernomas. The one exception is a possible cavernoma variant that occurs in the venous sinuses (intrasinus cavernoma) which has been reported to be susceptible to radiation (e.g., gamma knife or stereotactic radiosurgery). There is some debate over the precise pathology of this intrasinus cavernoma; i.e., it may be a variant of a cavernoma, or a different vascular lesion altogether!

In general, a cavernoma that is enlarging radiologically and/or symptomatic should be given consideration for surgery. Even ones located in the brainstem or spinal cord or other highly "eloquent" areas should be considered for removal if symptomatic and if relatively safely accessible surgically (i.e., ones that are causing neurological problems and present themselves to the surface of the brain or brain stem or spinal tissue region). The relative risks vs. benefits of surgery should be considered on an individual basis, and discussed comprehensively. Cavernomas in the brainstem and spinal cord and other highly "eloquent" regions require a highly experienced neurosurgeon for safe and effective treatment.

http://www.brain-aneurysm.com/cm.html

您參考一下，現在還有加碼刀能用(好羨慕)，注意第3點，這個有可能會遺傳