Juvenile idiopathic arthritis
Updates to Article Attributes
Juvenile idiopathic arthritis (JIA), also known asjuvenile rheumatoid arthritis, is the most common chronic arthritic disease of childhood and has multiple subtypes.
Epidemiology
The estimated incidence is ~13 per 100,000 per annum3. By definition, symptoms must start before 16 years of age. Females are more affected. F with a F:M ratio= 2 2:1.
Clinical presentation
Oligoarticular or polyarticular arthritis of of a duration of six weeks or longer must be present to diagnose JIA.
Patients may present with an acute onset of symptoms or a more gradual onset. Symptoms are often worse in the morning, but typically persist to some extent throughout the day.
In patients with systemic onset also known as Still disease, intermittent spiking fevers are typically noted, which help distinguish JIA from other diseases such as infection, other inflammatory diseases and malignancy. Migratory light light pink rash involving the trunk and/or extremities and hepatosplenomegaly are also also frequently observed in patients with systemic onset.
Radiographic features
Imaging shows a varied spectrum of involvement, based on the severity and duration of the disease.
RadiographPlain radiograph
Findings on x-ray include soft tissue swelling, osteopenia, loss of joint space, erosions, growth disturbances (epiphyseal overgrowth) and joint subluxation.
Hepatosplenomegaly may be seen on abdominal radiographs, and pericardial or pleural effusions may be seen on chest radiographs.
MRI
MRI shows synovial hypertrophy, joint effusions as well as osseous and cartilaginous erosions. Active synovitis is characterized by enhancement on T1-weighted gadolinium contrast studies.
-<p><strong>Juvenile idiopathic arthritis </strong>(<strong>JIA</strong>), also known as <strong>juvenile rheumatoid arthritis</strong> is the most common chronic arthritic disease of childhood and has multiple subtypes.</p><h4>Epidemiology</h4><p>The estimated incidence is ~13 per 100,000 per annum <sup>3</sup>. By definition, symptoms must start before 16 years of age. Females are more affected. F:M ratio= 2:1.</p><h4>Clinical presentation</h4><p>Oligoarticular or polyarticular arthritis of a duration of six weeks or longer must be present to diagnose JIA.</p><p>Patients may present with an acute onset of symptoms or a more gradual onset. Symptoms are often worse in the morning, but typically persist to some extent throughout the day.</p><p>In patients with systemic onset also known as<strong> Still disease</strong>, intermittent spiking fevers are typically noted, which help distinguish JIA from other diseases such as infection, other inflammatory diseases and malignancy. Migratory light pink rash involving the trunk and/or extremities and hepatosplenomegaly are also frequently observed in patients with systemic onset.</p><h4>Radiographic features</h4><p>Imaging shows a varied spectrum of involvement, based on the severity and duration of the disease.</p><h5>Radiograph</h5><p>Findings on x-ray include soft tissue swelling, <a href="/articles/regional-osteopaenia">osteopenia</a>, loss of joint space, erosions, growth disturbances (epiphyseal overgrowth) and joint <a href="/articles/subluxation">subluxation</a>.</p><p><a href="/articles/hepatosplenomegaly">Hepatosplenomegaly</a> may be seen on abdominal radiographs, and <a href="/articles/pericardial-effusion">pericardial</a> or <a href="/articles/pleural-effusion">pleural effusions</a> may be seen on chest radiographs.</p><h5>MRI</h5><p>MRI shows synovial hypertrophy, <a href="/articles/joint-effusion">joint effusions</a> as well as osseous and cartilaginous erosions. Active synovitis is characterized by enhancement on T1-weighted gadolinium contrast studies.</p>- +<p><strong>Juvenile idiopathic arthritis </strong>(<strong>JIA</strong>), also known as <strong>juvenile rheumatoid arthritis</strong>, is the most common chronic arthritic disease of childhood and has multiple subtypes.</p><h4>Epidemiology</h4><p>The estimated incidence is ~13 per 100,000 per annum <sup>3</sup>. By definition, symptoms must start before 16 years of age. Females are more affected with a F:M = 2:1.</p><h4>Clinical presentation</h4><p>Oligoarticular or polyarticular arthritis of a duration of six weeks or longer must be present to diagnose JIA.</p><p>Patients may present with an acute onset of symptoms or a more gradual onset. Symptoms are often worse in the morning, but typically persist to some extent throughout the day.</p><p>In patients with systemic onset also known as<strong> Still disease</strong>, intermittent spiking fevers are typically noted, which help distinguish JIA from other diseases such as infection, other inflammatory diseases and malignancy. Migratory light pink rash involving the trunk and/or extremities and hepatosplenomegaly are also frequently observed in patients with systemic onset.</p><h4>Radiographic features</h4><p>Imaging shows a varied spectrum of involvement, based on the severity and duration of the disease.</p><h5>Plain radiograph</h5><p>Findings on x-ray include soft tissue swelling, <a href="/articles/regional-osteopaenia">osteopenia</a>, loss of joint space, erosions, growth disturbances (epiphyseal overgrowth) and joint <a href="/articles/subluxation">subluxation</a>.</p><p><a href="/articles/hepatosplenomegaly">Hepatosplenomegaly</a> may be seen on abdominal radiographs, and <a href="/articles/pericardial-effusion">pericardial</a> or <a href="/articles/pleural-effusion">pleural effusions</a> may be seen on chest radiographs.</p><h5>MRI</h5><p>MRI shows synovial hypertrophy, <a href="/articles/joint-effusion">joint effusions</a> as well as osseous and cartilaginous erosions. Active synovitis is characterized by enhancement on T1-weighted gadolinium contrast studies.</p>