Everyone Healthy Library
Dermatomyositis
Condition / disease reference page from the Everyone Healthy database.
Connected health information
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Linked signs and symptoms
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Linked drugs / medications
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Treatments, therapies and supportive options
4Grouped by treatment type. These are educational database links, not personal treatment recommendations. Evidence labels are shown only where stored in the EH database.
Behavioural changes
2Linked diagnostic tests and investigations
6These are pulled from both EH diagnostic-test link tables, including the older large test-link table.
Biological and test markers
5This visual map uses existing EH database links to show biological agents and lab markers reported as increased, decreased, or associated with this condition. These are educational relationships only; test results must be interpreted by a qualified clinician because ranges vary by lab, method, age, sex and clinical context.
Often increased
4- Aspartate Aminotransferase (AST)Reference range exampleAdult ( > 16y), Female: 10–25 units/L; Adult ( > 16y), Male: 10–35 units/LLinked diagnostic tests1Aspartate Aminotransferase (AST) Concentration
- Cholesterol (Total)Reference range exampleInfant (0 - 1y): 75–180 mg/dL; Adult ( > 16y): 0–190 mg/dLLinked diagnostic tests1Cholesterol Concentration
- Creatine Kinase (CK)Reference range exampleAdult ( > 16y), Female: 35–150 units/L; Adult ( > 16y), Male: 40–170 units/LLinked diagnostic tests1Creatine Kinase Concentration
- MyoglobinReference range exampleAll: 5–85 ng/mLLinked diagnostic tests1Myoglobin Concentration
Often decreased
1Other associated markers
0No markers in this group.
Introduction / full article
Dermatomyositis
Dermatomyositis
Dermatomyositis is a disorder which frequently involves the muscle and skin manifesting as weakness or stiffness and purple to red skin discoloration. It may involve other organs like the lungs and esophagus. [1] [2]
Epidemiology
9.63 cases per million are recorded. Virtually any age can be affected. Two peaks are known. The first is during childhood usually during 5-10 years of age. The second peak is at adulthood around 50 years of age. Females are shown to have the condition more. [1]
Causes
The exact cause remains unknown. Genes are implicated to have an association in the development of the disease. Aberrations in immune system are common among patients. Viral infections are thought to be triggers in some cases. Among the organisms suspected are coxsackievirus, echovirus, HIV and Toxoplasma. Certain drugs are also thought to be likely causes such as penicillamine, hydroxyurea and statins. Some reports silicone breast implants or collagen injection as probable triggers although these are yet to be substantiated. [1]
Signs and Symptoms
One of the early symptoms is skin lesion. Commonly, it is a purple or red discoloration of the skin seen on typical locations like eyelids, knuckles, elbows or knees. After weeks or up to years, muscle involvement is observed. This is often noted as weakness of the proximal group of muscles. Patients may complain of climbing stairs, difficulty getting out of a chair or reaching for objects situated above them. The disease can involve other organs so that some patients may have arthritis, gastrointestinal ulcers, difficulty of swallowing and lung problems. Fatigue, fever and weight loss are also among the nonspecific symptoms of the disease. [3]
Diagnosis
After getting the patient’s history, the physician performs a physical examination which often involves searching for characteristic signs of the disease such as heliotrope and gottron papules. Laboratory exams may include getting the muscle enzyme levels, magnetic resonance imaging, muscle and skin biopsy, chest x-ray, ultrasonography and electromyography. [1]
Treatment
Medications that counteract the inflammation such as steroids are often prescribed. Some may be given immunosuppressant drugs like azathioprine. Calcinosis is common among pediatric patients. This can be removed through surgery.
References:
1. http://emedicine.medscape.com/article/332783-overview#a0101
2. http://www.nlm.nih.gov/medlineplus/ency/article/000839.htm
3. http://www.rheumatology.org/Practice/Clinical/Patients/Diseases_And_Conditions/Dermatomyositis_%28Juvenile%29/