Raynaud syndrome may be
Doctors use the term Raynaud syndrome to refer to either.
Primary Raynaud syndrome is much more common then secondary Raynaud syndrome. Between 60% and 90% of cases of primary Raynaud syndrome occur in women aged 15 to 40.
Anything that stimulates the sympathetic division of the autonomic nervous system, particularly exposure to cold but also strong emotion, can cause arteries to constrict and thus trigger primary Raynaud syndrome.
Secondary Raynaud syndrome may be caused by
Use of such drugs, which constrict blood vessels, can also make Raynaud syndrome worse. Some people with Raynaud syndrome also have other disorders that occur when arteries are prone to constrict. These disorders include migraines, variant angina (chest pain that occurs while at rest), and high blood pressure in the lungs (pulmonary hypertension). The association of Raynaud syndrome with these disorders suggests that the cause of arterial constriction may be the same in all of them.
Constriction of small arteries in the fingers and toes begins quickly, most often triggered by exposure to cold. It may last minutes or hours. The fingers and toes become pale (pallor) or bluish (cyanosis), usually in patches. Only one finger or toe or parts of one or more may be affected. The fingers or toes usually do not hurt, but numbness, tingling, a pins-and-needles sensation, and a burning sensation are common. As the episode ends, the affected areas may be redder than usual or bluish. Rewarming the hands or feet restores normal color and sensation.
If episodes of Raynaud syndrome recur and are prolonged (especially in people with systemic sclerosis), the skin of the fingers or toes may become smooth, shiny, and tight. Small painful sores may appear on the tips of the fingers or toes.
Usually, doctors suspect Raynaud syndrome on the basis of symptoms and results of the physical examination. Often, no procedures are needed to make the diagnosis. If doctors suspect an artery is blocked, Doppler ultrasonography may be done before and after the person is exposed to cold. Doctors may also order blood tests to check for conditions that can cause Raynaud syndrome.
People can control mild Raynaud syndrome by protecting their head, trunk, arms, and legs from cold. For those who experience symptoms when they get excited, mild sedatives or biofeedback may help. People who have the disorder must stop smoking because nicotine constricts blood vessels.
Primary Raynaud syndrome is commonly treated with a calcium channel blocker, such as nifedipine or amlodipine. Prazosin may also be effective.
For people with secondary Raynaud syndrome, doctors treat the disorder causing it.
Sympathectomy, a procedure in which certain sympathetic nerves may be temporarily blocked (by injection of a drug such as lidocaine) or even cut, may be used to relieve the symptoms of Raynaud syndrome if the disorder becomes progressively disabling and other treatments do not work. However, even when this procedure is effective, relief may last only 1 to 2 years. This procedure is usually more effective for people with primary Raynaud syndrome than for those with secondary Raynaud syndrome.
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