Juvenile Idiopathic Arthritis (page 4)

It may begin with a swollen knuckle, a spiking fever, or an unexplained rash. But no matter what symptoms appear, hearing the word "arthritis" in a diagnosis for your child can be unexpected and confusing.

Arthritis is an inflammation of the joints that is characterized by swelling, heat, and pain. Nearly 300,000 children in the United States have some sort of arthritis. Arthritis can be short-term — lasting for just a few weeks or months, then going away forever — or it can be chronic and last for months or years. In rare cases, it can last a lifetime.

The most prevalent form of juvenile arthritis is juvenile idiopathic arthritis (JIA) (also known as juvenile rheumatoid arthritis, or JRA). It affects about 50,000 U.S. kids and is very different from adult rheumatoid arthritis.

What Causes JIA?

It's not known exactly what causes JIA in kids. Research indicates that it is an autoimmune disease. In autoimmune diseases, white blood cells can't tell the difference between the body's own healthy cells and germs like bacteria and viruses. The immune system, which is supposed to protect the body from these harmful invaders, instead releases chemicals that can damage healthy tissues and cause inflammation and pain.

To effectively manage and minimize the effects of arthritis, an early and accurate diagnosis is essential. By understanding the symptoms and characteristics of each type of JIA, you can help your child maintain an active, productive lifestyle.

Types of JIA

JIA usually appears in kids between 6 months and 16 years old. The first signs often are joint pain or swelling and reddened or warm joints. Many rheumatologists (doctors specializing in joint disorders) find that the greater the number of joints affected, the more severe the disease and the less likely that the symptoms will eventually go into total remission.

There are seven major types of JIA:

1. Systemic JIA. Affects the whole body. Symptoms include high fevers that often increase in the evenings and then may suddenly drop to normal. During the onset of fever, the child may feel very ill, appear pale, or develop a rash. The rash may suddenly disappear and then quickly appear again. The spleen and lymph nodes might become enlarged. Eventually many of the body's joints are affected by swelling, pain, and stiffness.
   
2. Oligoarthritis. Affects four or fewer joints. Symptoms include pain, stiffness, or swelling in the joints. The knee and wrist joints are the most commonly affected. The two types of oligoarthritis, persistent and extended, are determined by how many joints are ultimately involved.
   
   Also, an inflammation of the iris (the colored area of the eye) may occur with or without active joint symptoms. This inflammation, called iridocyclitis, iritis, or uveitis, can be detected early by an ophthalmologist.
3. Polyarticular arthritis, rheumatoid factor negative. Affects more girls than boys. Symptoms include swelling or pain in five or more joints. The small joints of the hands are affected as well as the weight-bearing joints like the knees, hips, ankles, feet, and neck.
   
   A low-grade fever also might develop, as well as bumps or nodules in areas of the body subjected to pressure from sitting or leaning.
   
4. Polyarticular arthritis, rheumatoid factor positive. Affects about 15% of kids with polyarticular arthritis or about 3% of all children with JIA. This type of JIA behaves the most like adult rheumatoid arthritis, and kids are at a higher risk of joint damage with erosions than in the other forms of JIA.
   
5. Psoriatic arthritis. Kids with this also have the psoriasis rash themselves or a close relative with psoriasis. Their fingernails and/or toenails might be affected by the condition.
6. Enthesitis-related arthritis. Most commonly affects the lower extremities and the spine. Kids also might have inflammation where tendons join bones (e.g., where the Achilles tendon attaches to the back of the heel).
   
   Enthesitis-related arthritis includes a special group call juvenile ankylosing spondylitis (where joints of the low back are inflamed) and arthritis associated with inflammatory bowel disease (Crohn's disease and ulcerative colitis).
   
7. Undifferentiated arthritis. Arthritis that doesn't fit into any of the above categories or fits into more than one of the categories.

The first signs of arthritis, which can be subtle or obvious, include limping or a sore wrist, finger, or knee. Joints may suddenly swell and remain enlarged. Stiffness in the neck, hips, or other joints also can occur.

Rashes may suddenly appear and disappear, developing in one area and then another. High fevers that tend to spike in the evenings and suddenly disappear are characteristic of systemic JIA.

Diagnosis

To diagnose JIA, the doctor will take a detailed medical history and conduct a thorough physical examination. The doctor may order X-rays or blood tests to rule out other conditions or infections, such as Lyme disease, that may cause similar symptoms or occur along with the arthritis.

Other tests done can include:

• CBC (complete blood count), a common blood test used to evaluate all the basic cellular components of blood, including red blood cells, white blood cells, and platelets. Abnormalities in the numbers and appearances of these cells can be useful in the diagnosis of many medical conditions.
• Blood culture, a test to detect bacteria that cause infections in the bloodstream. This may be done to rule out infections.
• Bone marrow examination, a test that allows doctors to look at blood where it's formed (in the bone marrow) to rule out conditions such as leukemia.
• Erythrocyte sedimentation rate, which checks how rapidly red blood cells settle to the bottom of a test tube. This rate often increases in people when inflammation is occurring in the body.
• A test for rheumatoid factor (RF) and cyclic citrullinated peptide antibody (CCP), antibodies produced in the blood of children with some forms of JIA. But it's much more commonly found in adults with rheumatoid arthritis.
• ANA (antinuclear antibody), a blood test to detect autoimmunity. It's also useful in predicting which kids are likely to have eye disease with JIA.
• A bone scan, to detect changes in bone and joints to evaluate the causes of unexplained bone and joint pain.

In some cases, the doctor may want an orthopedic surgeon to examine your child's joints and take samples of joint fluid or synovium (the lining of the joints) for examination and testing.

Treatments

In many cases, JIA is treated with a combination of medication, physical therapy, and exercise. In some cases, a child may require corticosteroid injections into the joint or surgery. The health care providers, including the primary care physician, rheumatologist, and physical therapist, will work together to develop the best method of treatment.

The goals of treatment are to relieve pain and inflammation, slow down or prevent the destruction of joints, and restore use and function of the joints to promote optimal growth, physical activity, and social and emotional development.