Mixed connective tissue disease

Overview

Mixed connective tissue disease (MCTD) has signs and symptoms of a combination of disorders — primarily lupus, scleroderma, and polymyositis. Many people with this uncommon disease also have Sjogren's syndrome. For this reason, MCTD is sometimes called an overlap disease.

In mixed connective tissue disease, the symptoms of the separate diseases usually don't appear all at once. Instead, they tend to occur over a number of years, which can complicate diagnosis.

Early signs and symptoms often involve the hands. Fingers might get puffy, and the fingertips become white and numb, often in response to cold exposure. In later stages, some organs — such as the lungs, heart and kidneys — can be affected.

There's no cure for mixed connective tissue disease. Treatment depends on how severe the disease is and the organs involved.

Symptoms

Early indications of mixed connective tissue disease can include:

General feeling of being unwell. This can include increased fatigue and a mild fever.
Cold and numb fingers or toes (Raynaud's phenomenon). In response to cold or stress, your fingers or toes might turn white and then purplish blue. After warming, the fingers or toes turn red.
Swollen fingers or hands. Some people have swelling of the fingers.
Muscle and joint pain. Joints can become inflamed, swollen and deformed, similar to what occurs with rheumatoid arthritis.
Rash. Red or reddish brown patches can appear over the knuckles.

When to see a doctor

See your doctor if you have signs and symptoms that interfere with your daily routine — particularly if you've been diagnosed with lupus or another connective tissue disease.

Causes

Mixed connective tissue disease is an autoimmune disorder, although the cause isn't known. In autoimmune disorders, your immune system — responsible for fighting off disease — mistakenly attacks healthy cells.

In connective tissue diseases, your immune system attacks the fibers that provide the framework and support for your body. Some people with mixed connective tissue disease have a family history of the condition. But the role of genetics in the disease remains unclear.

Risk factors

Mixed connective tissue disease can occur in people of any age. However, it appears to be most common in women under the age of 50.

Complications

Mixed connective tissue disease can lead to serious complications, some of which can be fatal. Complications include:

High blood pressure in the lungs (pulmonary hypertension). This condition is a major cause of death in people with mixed connective tissue disease.
Interstitial lung disease. This large group of disorders can cause scarring in your lungs, which affects your ability to breathe.
Heart disease. Parts of the heart can enlarge, or inflammation can occur around the heart. Heart failure can occur.
Kidney damage. About one-fourth of people with mixed connective tissue disease develop kidney problems, Kidney involvement is usually mild, but can lead to kidney failure.
Digestive tract damage. Commonly, mixed connective tissue disease affects the digestive tract. You might have abdominal pain and problems with swallowing and digesting food.
Anemia. About 75% of people with mixed connective tissue disease have iron deficiency anemia.
Tissue death. People with severe Raynaud's disease can develop gangrene in the fingers.
Hearing loss. In one small study, hearing loss was reported in almost half the patients with mixed connective tissue disease. More research is needed to understand this association.
Nerve damage. Sjogren syndrome can affect the nerve that carries feeling from your face to your brain (trigeminal nerve). If you have trigeminal neuralgia, even mild stimulation of your face — such as from brushing your teeth or putting on makeup — can trigger a jolt of severe pain.

Diagnosis

During the physical exam, your doctor may check you for swollen hands and painful, swollen joints. You might also need a blood test to check for a certain antibody that is associated with mixed connective tissue disease.

Treatment

There's no cure for mixed connective tissue disease. Medication can help manage the signs and symptoms.

The type of medication prescribed depends on the severity of your disease and your symptoms. Medications can include:

Corticosteroids. Drugs, such as prednisone (Deltasone, Rayos), can help prevent your immune system from attacking healthy cells and suppress inflammation. Side effects of corticosteroids can include mood swings, weight gain, high blood sugar, increased blood pressure, weakened bones and cataracts.
Antimalarial drugs. Hydroxychloroquine (Plaquenil) can treat mild mixed connective tissue disease and might prevent flare-ups.
Calcium channel blockers. This category of medications, including nifedipine (Adalat CC, Procardia) and amlodipine (Norvasc), that help relax the muscles in the walls of your blood vessels might be used to treat Raynaud's phenomenon.
Other immunosuppressants. Your doctor might prescribe other medications based on your signs and symptoms. For example, if they're similar to those of lupus, your doctor might recommend medications typically prescribed for people with lupus.
Pulmonary hypertension medications. Bosentan (Tracleer) or sildenafil (Revatio, Viagra) might be prescribed.

Self care

Other ways to control symptoms of mixed connective tissue disease include:

Nonsteroidal anti-inflammatory drugs. These medications, such as ibuprofen (Advil, Motrin IB, others) or naproxen sodium (Aleve), might help relieve the pain and inflammation if your condition is mild.
Protecting hands from cold. Wearing gloves and taking other measures to keep your hands warm can help prevent Raynaud's phenomenon.
Not smoking. Smoking causes blood vessels to narrow, which can worsen the effects of Raynaud's phenomenon.
Reducing stress. Raynaud's phenomenon is often triggered by stress. Relaxation techniques — such as slowing and focusing on your breathing — can help reduce your stress levels.

Preparing for your appointment

You might be referred to a doctor who specializes in joint diseases (rheumatologist).

What you can do

Have a friend or relative accompany you to your appointment to help you retain the information you get.

Make a list of:

Your symptoms, including any that may seem unrelated to the reason why you scheduled the appointment, and when they began
Key medical information, including other conditions you have and whether anyone in your family has had similar problems
All the medications, vitamins or other supplements you take, including doses
Questions to ask your doctor

Some basic questions you might want answered include:

What's the most likely cause of my symptoms?
What tests do I need?
What treatments are available?
I have other health conditions. How can I best manage them together?

Don't hesitate to ask other questions.

What to expect from your doctor

Your doctor is likely to ask you questions, such as:

Have your symptoms been continuous or occasional?
How severe are your symptoms?
What, if anything, seems to improve or worsen your symptoms?