Susac's syndrome is a rare, autoimmune disease. "Autoimmune" means that a person's immune system mistakenly attacks the person's own tissues. In Susac's syndrome, the immune system attacks the smallest blood vessels in the brain, retina (part of the eye), and inner ear. The blood vessels become blocked. Problems in the brain, retina, and inner ear occur due to decreased blood flow.
Susac's syndrome is rare, but when it occurs it strikes mainly females between the ages of 20 and 40. However, children as young as 8 and adults (both men and women) into their 50s can be affected.
Inner ear symptoms:
All three parts of the disease may not appear at the same time. Any one of the above symptoms may be the first sign of Susac's syndrome. It may take weeks, months, or even years for all three parts to show up, and some patients never have more than two of them.
Susac's syndrome is caused by a person's own immune system attacking the endothelial cells— the cells that line the inner walls of our blood vessels—in the brain, retina, and inner ear. When attacked, the endothelial cells swell up and partly or completely shut off blood flow through the vessel. The resulting lack of oxygen and nutrients causes the affected organs to suffer.
What causes the immune system to malfunction in this way is not known.
A neurological exam may find that the patient has:
Magnetic resonance imaging (MRI) may find:
Fluorescein angiography looks at blood flow in the eye. Findings in Susac's syndrome include:
A hearing test may find:
Because its symptoms are similar to those of a number of other diseases—such as multiple sclerosis, ADEM, encephalitis, meningitis, lupus, and CNS vasculitis—Susac's syndrome may be difficult to diagnose.
Susac's syndrome is best treated as soon as possible with an aggressive, long-term course of drugs that suppress the immune system, such as steroids. Medications may include:
Some doctors recommend that Susac's syndrome patients avoid the use of oral contraceptives and estrogen-replacement therapies because hormones may aggravate the blockage of blood vessels.
The immunosuppressive drugs give the body a chance to correct itself while slowing down the immune system's attacks. As this correction takes place, the dosage of drugs can be decreased. The patient should be watched so that drug levels are kept in balance with the rate at which the immune system stabilizes. If treatment is discontinued too quickly, the disease may flare up again.
There is no way to prevent Susac's syndrome because the autoimmune response that causes it has not been identified.
Susac's syndrome may follow a different path for everyone. In some people, the syndrome disappears in a few months, even without treatment. In others, symptoms keep coming back even after long-term treatment.
Susac's syndrome usually lasts between six months and five years. Most patients seem to get better after about two to four years. If the symptoms during this period are mild or easily controlled with medications, there may be little or no lasting damage. Some people, however, have severe cases in which there is permanent harm, including dementia, loss of vision, and deafness. Susac's syndrome can also reappear after many years of remission.
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This information is provided by the Cleveland Clinic and is not intended to replace the medical advice of your doctor or healthcare provider. Please consult your healthcare provider for advice about a specific medical condition. This document was last reviewed on: 05/26/2017