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Cavernous Angioma

Also known as: Cavernoma; Cavernous Malformation

What is it?

Cavernous angiomas are a type of vascular malformation of the brain. Cavernomas consist of a collection of slow flow vessels under low pressure and contain no large feeding arteries or large draining veins. They are prone to small recurrent hemorrhages. A majority of cavernomas are found in the brain but they also can be seen in the spinal cord.

Who gets it?

Cavernous angiomas are often sporadic in nature. They can be hereditary with variable expressivity.

What causes it?

It is not known what causes cavernous angiomas.

What are the symptoms?

Patients with cavernous angiomas are often times without symptoms. Patients often present with a history of seizures or progressive neurological deficit secondary to the small hemorrhages.

How is it diagnosed?

Cavernous angiomas are best seen on specific sequences on brain MRI studies. CAT scans can demonstrate these lesions if there is a predominance of calcification. Cavernomas are known as angiographically occult vascular malformations and are not seen on diagnostic cerebral angiography.

What is the treatment?

Cavernous angiomas can be treated by two options. Microsurgery is the treatment of choice for lesions that are symptomatic and accessible. Removal of these cavernous angiomas at surgery eliminates the risk of bleeding. In the case of epilepsy, surgery may cure or at least reduce the severity of seizures. Since cavernous angiomas are not visible on an angiogram, endovascular embolization is not possible. Stereotactic radiosurgery may have a role in the treatment of some deep or inaccessible lesions


This information has been designed as a comprehensive and quick reference guide written by our health care reviewers.  The health information written by our authors is intended to be a supplement to the care provided by your physician.  It is not intended nor implied to be a substitute for professional medical advice. 

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This page was last updated on April 05, 2007
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