Hi, i have the Raynaud syndrome and i wanted to know if this "illness" may lead to any other health problem...

Thanks!

Answer:
It can be very serious if not managed properly. Please discuss this with your doctor and take the medication that s/he prescribes to increase blood flow to the affected areas. My mother had it and was helped by wearing gloves especially whenever she had to handle anything cold.

You can read up on it at the website I reference below:
Well, I don't know about Raynaud, but I have about 3 or 4 different health issues and my advice to you is to research it. Here are a few places to get you started:
Raynaud’s phenomenon is a condition that affects the blood vessels in the extremities—generally, the fingers and toes. It is characterized by episodic attacks, called vasospastic attacks, in which the blood vessels in the digits (fingers and toes) constrict (narrow), usually in response to cold temperatures and/or emotional stress. When this condition occurs on its own, it is called primary Raynaud’s phenomenon. When it occurs with another condition such as scleroderma or lupus, it is called secondary Raynaud’s phenomenon.

Most people with Raynaud’s phenomenon have the primary form, which is not associated with any underlying disease. In fact, in these individuals it is thought to be an exaggeration of normal responses to cold temperature and/or stress.

When Raynaud’s phenomenon is caused by or associated with an underlying disease, it is referred to as secondary Raynaud’s phenomenon. Secondary Raynaud’s phenomenon tends to begin later in life than the primary form, typically after 35 to 40 years of age.

It is common for patients with a connective tissue disease to have Raynaud’s phenomenon. It occurs in more than 90 percent of patients with scleroderma, and in about 30 percent of patients with systemic lupus erythematosus and with Sjögren’s syndrome. Secondary Raynaud’s phenomenon may also be associated with exposure to vibrating tools such as jackhammers, which cause trauma to the hands and wrists. And it may be linked to certain drugs, such as chemotherapy agents, or to chemicals such as vinyl chloride.

In medical literature, primary Raynaud’s phenomenon may also be called idiopathic Raynaud’s phenomenon, primary Raynaud’s syndrome, or Raynaud’s disease. There is no known cause for primary Raynaud’s phenomenon. It is more common than the secondary form and often is so mild the patient never seeks medical attention. It generally is an annoyance that causes little disability. Secondary Raynaud’s phenomenon is a more complex and serious disorder.

The most common cause of secondary Raynaud’s phenomenon is connective tissue disease. The condition most commonly occurs with scleroderma or lupus, but is also associated with Sjögren’s syndrome, dermatomyositis, and polymyositis. Some of these diseases reduce blood flow to the fingers and toes by causing blood vessel walls to thicken and the vessels to constrict too easily.

Other possible causes of secondary Raynaud’s phenomenon are carpal tunnel syndrome and obstructive arterial disease (blood vessel disease). Some drugs are also linked to Raynaud’s phenomenon. They include beta-blockers, such as Lopressor1 or Cartrol, used to treat high blood pressure; ergotamine preparations, such as Cafergot or Wigrane, used for migraine headaches; certain agents used in cancer chemotherapy; and drugs, such as over-the-counter cold medication and narcotics, that cause vasoconstriction.

People in certain occupations may be more vulnerable to secondary Raynaud’s phenomenon. Some workers in the plastics industry who are exposed to vinyl chloride, for example, develop a scleroderma-like illness, of which Raynaud’s phenomenon can be a part. Workers who operate vibrating tools can develop a type of Raynaud’s phenomenon called vibration-induced white finger.

Severe cases of Raynaud’s phenomenon—usually of the secondary form—can lead to problems such as skin ulcers (sores) or gangrene (tissue death) in the fingers and toes, which can be painful and difficult to treat.

Most doctors find it fairly easy to diagnose Raynaud’s phenomenon but find it more difficult to identify the form of the disorder.

Physicians can now distinguish primary from secondary Raynaud’s phenomenon with a complete history and physical examination. Sometimes, special blood testing is needed. If the evaluation and special testing studies are normal, then the diagnosis of primary Raynaud’s phenomenon can be made and it is unlikely to change into a secondary form. Interestingly, about 30 percent of first-degree relatives of patients with primary Raynaud’s phenomenon also have the condition. This finding suggests that primary Raynaud’s phenomenon is determined by some yet-to-be discovered genetic trait.

A few tests can help the doctor distinguish between primary and secondary Raynaud’s phenomenon. They are:

Nailfold capillaroscopy—During this test, the doctor puts a drop of oil on the patient’s nailfolds, the skin at the base of the fingernail. The doctor then examines the nailfolds under a microscope to look for problems in the tiny blood vessels called capillaries. If the capillaries are enlarged or malformed, the patient may have a connective tissue disease.

Antinuclear antibody (ANA) test—In this blood test, the doctor determines whether the body is producing special proteins called antibodies that are directed against the nuclei of the body’s cells. These abnormal antibodies are often found in people who have connective tissue diseases or other autoimmune disorders.

Erythrocyte sedimentation rate (ESR or sed rate)—This is a laboratory test for inflammation that measures how quickly red blood cells fall to the bottom of a test tube of unclotted blood. Rapidly descending cells (an elevated sed rate) indicate inflammation in the body.

What Is the Treatment for Raynaud’s Phenomenon?

The aims of treatment are to reduce the number and severity of attacks and to prevent tissue damage and loss of tissue in the fingers and toes. Most doctors are conservative in treating patients with primary Raynaud’s phenomenon because they do not get tissue damage. For these patients, doctors tend to recommend nondrug treatments before moving onto medications. For patients with secondary Raynaud’s phenomenon, medications are more often prescribed, because severe attacks with ulcers or tissue damage are more likely.

In the most severe cases, Raynaud’s causes ulcers and serious tissue damage that does not respond to medications. Doctors may use a surgical procedure called a digital sympathectomy with adventitial stripping (which involves removing the tissue and nerves around the blood vessels supplying the affected digits). While this procedure may result in reducing symptoms and healing tissue, it only helps temporarily and therefore is reserved for difficult cases.

The medicine and health information post by website user , ByeDR.com not guarantee correctness , is for informational purposes only and is not a substitute for medical advice or treatment for any medical conditions.


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