Juvenile idiopathic arthritis

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Juvenile idiopathic arthritis
Synonyms	Juvenile rheumatoid arthritis, juvenile chronic arthritis
Pronounce	N/A
Specialty	N/A
Symptoms	Joint pain, swelling, stiffness, fever, rash
Complications	Uveitis, growth problems, joint damage
Onset	Before age 16
Duration	Chronic
Types	N/A
Causes	Unknown, possibly autoimmune disease
Risks	Family history, certain genetic factors
Diagnosis	Clinical evaluation, blood tests, imaging
Differential diagnosis	Infection, trauma, other autoimmune diseases
Prevention	N/A
Treatment	Nonsteroidal anti-inflammatory drugs, corticosteroids, disease-modifying antirheumatic drugs, physical therapy
Medication	N/A
Prognosis	Variable, some achieve remission, others may have chronic symptoms
Frequency	1 in 1,000 children
Deaths	N/A

Juvenile Idiopathic Arthritis

Juvenile Idiopathic Arthritis (JIA) is a type of arthritis that occurs in children aged 16 or younger. It is characterized by persistent joint inflammation, which can lead to joint damage and other complications if not treated effectively.

Classification

Juvenile Idiopathic Arthritis is classified into several subtypes based on symptoms, number of joints involved, and the presence of certain antibodies. The main subtypes include:

• Oligoarticular JIA: Involves four or fewer joints in the first six months of the disease.
• Polyarticular JIA: Affects five or more joints in the first six months and can be rheumatoid factor positive or negative.
• Systemic JIA: Characterized by arthritis, fever, and rash.
• Enthesitis-related arthritis: Involves inflammation of the entheses, the sites where tendons or ligaments insert into the bone.
• Psoriatic arthritis: Associated with psoriasis, a skin condition.

Symptoms

The symptoms of Juvenile Idiopathic Arthritis can vary depending on the subtype but generally include:

• Joint pain and swelling
• Stiffness, especially in the morning
• Fever and rash (in systemic JIA)
• Fatigue
• Reduced range of motion

Diagnosis

Diagnosing JIA involves a combination of clinical evaluation, laboratory tests, and imaging studies. Key diagnostic criteria include:

• Persistent arthritis in one or more joints for at least six weeks
• Exclusion of other causes of arthritis
• Laboratory tests such as antinuclear antibody (ANA), rheumatoid factor (RF), and HLA-B27
• Imaging studies like X-ray or MRI to assess joint damage

Treatment

The treatment of Juvenile Idiopathic Arthritis aims to control symptoms, prevent joint damage, and maintain function. Treatment options include:

• Nonsteroidal anti-inflammatory drugs (NSAIDs) for pain and inflammation
• Disease-modifying antirheumatic drugs (DMARDs) such as methotrexate
• Biologic agents like tumor necrosis factor inhibitors
• Corticosteroids for severe inflammation
• Physical therapy to maintain joint function

Prognosis

The prognosis for children with Juvenile Idiopathic Arthritis varies. Some children may experience remission, while others may have persistent symptoms into adulthood. Early diagnosis and treatment are crucial for improving outcomes.

Complications

Potential complications of JIA include:

• Joint damage and deformity
• Growth disturbances
• Uveitis, an inflammation of the eye
• Osteoporosis due to prolonged corticosteroid use

See Also

• Arthritis
• Autoimmune disease
• Pediatric rheumatology

External Links

• [Juvenile Idiopathic Arthritis Foundation]
• [American College of Rheumatology]

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