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Cavernous Malformations

Cavernous Malformations

Cavernous malformations are also known as cavernous angiomas, cavernous hemangiomas, cerebral cavernous malformations or cavernomas.

It is a condition in which clusters of blood vessels in your child’s brain or spinal cord form abnormally, creating ‘caverns’ filled with slow-moving blood.

Some cavernous malformations cause no symptoms, but larger cavernomas may cause headaches, seizures, and impaired speech or vision.

What is a Cavernous Malformation?

A cavernous malformation is group of small blood vessels (capillaries) in the brain that binds together to form a small tunnel of blood in the brain.

The malformations can vary in size. They may be as small as a pea or up to 5 inches long.

Blood inside a cavernoma does not circulate normally. It often moves very slowly. As the volume of blood inside the cavernoma increases, it may grow in size and push on other areas of the brain, causing a variety of symptoms.

Because small blood vessels have thinner walls than other larger vessels, their expansion to hold too much blood may even cause them to burst and bleed inside the brain. Your neurosurgeon may suggest surgery if the cavernous malformation is bleeding into the brain or pushing on certain parts of the brain.

Symptoms of Cavernous Malformation

Symptoms arise when the cavernoma either presses on another area of the brain or begins to bleed.

Symptoms may include one or more of the following:

  • Headaches
  • Seizures
  • Trouble speaking
  • Vision changes
  • Balance problems
  • Weakness or numbness in arms or legs
  • Gradual or sudden changes in personality

Most cases of cavernoma bleeding involve very small amounts of blood that may not cause any symptoms.

If there is a larger amount of bleeding, symptoms will develop more quickly. This potentially life-threatening situation requires immediate treatment.

What Causes a Cavernous Malformation?

Approximately 1 in 4 cases of cavernous malformation are inherited. The remaining cases have no clear cause.

Individuals with inherited cavernous malformations are more likely to have multiple cavernomas in the brain, increasing their risk of developing symptoms. Half of the people who inherit cavernous malformations will pass the condition on to their children.

Non-inherited cases often result in just one cavernoma with few or no symptoms.

How Common are Cavernous Malformations?

Cavernous malformations occur in less than 1 in 1,000 births. Most children and adults with non-inherited cavernomas never have symptoms and often go undiagnosed. If an individual does have symptoms, they typically develop before the age of 30.

Cavernous malformations affect all ethnic groups. Females and males have equal chance of having the disease.

Diagnosis of a Cavernous Malformation

In order to properly diagnose and locate cavernous malformations, magnetic resonance imaging (MRI) or computed tomography (CT) may be used to see two- or three-dimensional images of the brain. These tests will identify cavernomas and often show any bleeding that may have occurred.

Treatment and Surgery

The goal of treatment is to:

  • identify and surgically handle life-threatening cases of cavernous malformation
  • relieve symptoms in patients with non-life-threatening cavernous malformations.

In cases of severe cavernoma bleeding, our Neurosurgery team is prepared 24 hours a day to provide urgent surgical intervention.

In non-life-threatening cases, our team will first verify that your child’s symptoms are truly caused by the cavernous malformation(s) before suggesting specific treatment. If your child has multiple cavernomas, we will observe your child to attempt to identify whether one or more cavernomas are causing the symptoms.

If surgery is recommended, our surgeon will explain the location of the cavernoma(s) and identify potential risks of surgical removal. Together you will determine the best course of action, weighing the risks of keeping the cavernous malformation against the risks of doing surgery.

There are currently no drug treatments for cavernous malformations; however there are drug treatments to alleviate symptoms such as seizures or headache.

Possible Risks and Complications of Surgery

As with any surgical procedure, there are possible complications. Risks are rare given modern surgical methods practiced by our experienced neurosurgeons. Risk levels vary upon the location of the cavernoma(s) in the brain.

Most complications with cavernous malformations are neurological in nature. Complications may include:

  • Stroke
  • Paralysis
  • Coma
Such complications may require additional treatment and/or surgery. Our team of specialists are prepared to address any of these rare complications and will help your family weigh these risks carefully when considering surgery.

Recovery

Your surgeon will provide specific instructions during your child’s recovery period. Most children are able to leave the hospital within one week of surgery. Your child may return to normal life within a month following surgery. Doctors will continue to monitor your child’s condition in the following weeks and months.

If other neurological problems arise, your child may receive additional treatment from a variety of specialists (neurologists, physical therapists, speech therapists, etc.).

Prognosis

Long-term outlook is good for most children with one or more cavernous malformations. They typically go on to live normal lives.

It is difficult to identify specific causes of bleeding in the brain. Your physician may recommend avoidance of high-impact sports and activities that may result in significant head trauma.

Last Updated 06/2019

Who Treats This

Who treats this?

The Cerebrovascular Disease and Stroke Center at Cincinnati Children’s treats all vascular diseases of the brain and spine.

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Contact the Cerebrovascular Disease and Stroke Center at 513-636-4726 to make an appointment or for information.

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