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Autoimmune Conditions

Mixed Connective Tissue Disease (MCTD)

Other Names: Sharp's Syndrome, Undifferentiated Connective Tissue Disease, Commonly referred to as an “Overlapping Disease”

Mixed Connective Tissue Disease is an uncommon autoimmune disease involving the connective tissues that make up the support for your body's structure. Connective tissues include skin, muscle, cartilage, tendons, ligaments, and fat to name a few.MCTD is actually a generalized diagnosis that is made up of a few overlapping connective tissue autoimmune diseases. The term Mixed Connective Tissue Disease is usually diagnosed when none of the symptoms or signs of one of the connective tissue diseases is not prominent enough to diagnose just one connective tissue disease (hence the term mixed connective tissue).

The most common connective tissue diseases involved in MCTD include:

Scleroderma
Myositis
Systemic Lupus Erythematosus
Rheumatoid Arthritis

Some of the initial symptoms of MCTD might include joint pain, swelling, malaise (generally just not feeling well), dry skin, muscle inflammation and thickening of the skin on the pads of your fingers. You may also experience Raynaud's Phenomenon for months to years before any symptoms begin to develop.

Usually not all of the symptoms will develop at once. It's a slow, progressive disease that can take months to years to develop to a point where doctors can pinpoint and diagnose the disease. As time passes, more signs and symptoms will develop and eventually one of the connective tissue diseases may become dominant enough for a conclusive diagnosis. In other cases, that may never be possible and the diagnosis of MCTD will stay the final diagnosis.

MCTD most commonly strikes women in there 20-30's, however children have also been known to develop the disease. Left untreated, MCTD can cause complications ranging from pulmonary hypertension, heart disease, pregnancy complications and of course side effects from medications used to treat MCTD.

Symptoms:

Abdominal cramps
Abdominal pain
Abdominal tenderness
Difficulty chewing
Difficulty swallowing
Dry cough
Frequent heartburn
General joint pain and stiffness
Hoarse voice
Pain in hips
Rash across nose and cheeks
Shoulder pain
Swelling in hands and fingers
Swollen lymph nodes
Unusual hair loss in small patches

Diagnosis:

If a doctor suspects MCTD, a thorough exam and symptom medical review will be performed. Blood tests may also show:

Positive Lupus Anticoagulant Antibody
Elevated Small Nuclear Ribonucleoprotein 70kDa Polypeptide
Positive Anti-Nuclear Antibody
Positive Anti-Phospholipid Antibody
Positive Rheumatoid Factor
Elevated Rheumatoid Factor Quantity
Low Total Serum Iron
Elevated Anti-Ribonucleoprotein Antibody


Imaging (X-rays, CT Scans and MRI among others) may also be used to determine damage being done to tissues and organs


Treatment:

There is no cure for MCTD and mild forms of it may not need treatment at all. Non-Steroidal Anti-Inflammatories such as Naproxen and Ibuprofen may be used to reduce inflammation. Patients not responding to NSAID's or not able to tolerate NSAID's due to stomach conditions, bouts of Corticosteroids may be used to reduce inflammation and the immune response.

Immunosuppressant therapy may also be used to reduce the immune response causing the healthy tissue to be attacked, and many of the therapy options used to treat Scleroderma, Myositis, SLE and Rheumatoid Arthritis may also be used to treat MCTD.

Prognosis:

With proper treatment, support and lifestyle adjustments, the prognosis of MCTD is relatively good. It is important to follow your therapy and find support, especially when the disease is active, whether it includes medication or alternative medicine. Properly caring for yourself can improve the quality of life for MCTD sufferers.

 

 
 
 

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