Scleroderma/morphea

There are two forms of scleroderma: localized scleroderma and systemic sclerosis. Localized scleroderma can be seen more frequently in children than the systemic form. It may involve patches of the skin on the trunk, arms, legs, or head. Other names for the localized form are morphea and linear scleroderma.

Symptoms of localized scleroderma may include:

• shiny, thickened patches of skin
• discolored (lighter or darker) skin
• joint tightness

Scleroderma is considered to be a multifactorial condition. Multifactorial inheritance means that "many factors" are involved in causing a health problem. The factors are usually both genetic and environmental, where a combination of genes from both parents, in addition to unknown environmental factors, produce the trait or condition. Often one gender (either males or females) is affected more frequently than the other in multifactorial traits. Females are affected with scleroderma three to four times more often than males.

What are the symptoms of systemic sclerosis?

Systemic sclerosis can lead to scarring of the skin, joints, and other internal organs. In systemic sclerosis there is also a syndrome known as CREST. In CREST syndrome, you may see calcium deposits in the skin, esophageal dysfunction and lung involvement that can lead to heart and respiratory failure.

Symptoms of scleroderma may resemble other medical conditions or problems. Always consult your child's physician for a diagnosis.

• thickening and swelling of the tips of the fingers
• pale and tingly fingers that may become numb when exposed to cold or when emotionally upset (called Raynaud phenomenon)
• joint pain
• morning stiffness
• taut, shiny, darker skin on large areas such as the face, that may hinder movement
• appearance of spider veins
• calcium bumps on the fingers or other bony areas
• grating noise as inflamed tissues move
• frozen (immobile) fingers, wrists, or elbows due to scarring of the skin
• sores on fingertips and knuckles
• scarring of the esophagus, leading to heartburn and difficulty swallowing
• scarring of the lungs, leading to shortness of breath
• heart failure and abnormal heart rhythms
• kidney disease

How is scleroderma diagnosed?

Diagnosis of scleroderma is usually based on the changes in the skin and internal organs. An antibody test may help distinguish the type of scleroderma present. In addition to a complete medical history and physical examination, diagnostic procedures for scleroderma may include:

• electrocardiogram (EKG or ECG) - a test that records the electrical activity of the heart, shows abnormal rhythms (arrhythmias or dysrhythmias), and detects heart muscle damage. An EKG may be done to detect changes in the EKG pattern which may be caused by changes in the heart muscle tissue due to scleroderma.
• echocardiogram - a procedure that evaluates the structure and function of the heart by using sound waves recorded on an electronic sensor that produce a moving picture of the heart and heart valves.
• x-ray - a diagnostic test which uses invisible electromagnetic energy beams to produce images of internal tissues, bones, and organs onto film. X-rays may detect changes in bone and soft tissues, the gastrointestinal tract, and the lungs caused by scleroderma.

Treatment for scleroderma:

Specific treatment for scleroderma will be determined by your child's physician based on:

• your child's overall health and medical history
• extent of the condition
• your child's tolerance for specific medications, procedures, and therapies
• expectation for the course of the disease
• your opinion or preference

Treatment may include:

• nonsteroidal, anti-inflammatory medications (NSAIDs) or corticosteroids (to relieve pain)
• immunosuppressive medications, such as methotrexate
• treating specific symptoms, such as heartburn and Raynaud phenomenon
• physical therapy and exercise (to maintain muscle strength)