Corticosteroids

Corticosteroids are hormones that play a role in stress and immune response as well as blood electrolyte levels. Corticosteroids prevent production of prostaglandins that cause inflammation and allergy. But they interfere with the white blood cell functioning and make an individual more prone to infections. Corticosteroids are used to control inflammations such as rheumatoid arthritis, ankylosing spondylitis, asthma, hepatitis and lupus. Side effects of long-term use of corticosteroids are water retention, diabetes, osteoporosis, high blood pressure, stomach ulcers and depression.

Steroids

Steroids are either anabolic or corticosteroids. Anabolic steroids are synthetic hormones that increase the levels of testosterone in the blood. Corticosteroids are drugs that are prescribed for inflammation. Anabolic steroids are largely taken by those who are seeking to increase muscle mass, especially athletes and bodybuilders. But these kind of steroids are not without side-effects. Prolonged use can lead to reproductive problems. Women athletes who take anabolic steroids over a long period of time also face problems such as voice deepening, acute acne, increased facial and body hair. Other effects of long-term steroid use are liver tumors, blood lipid abnormality, enlarged heart muscles and growth of breasts in men.

Polymyositis

Polymyositis is a chronic inflammatory disease of the skeletal muscle. It is a predominant form of muscular dystrophy, noticed among elderly people. It is categorized as one of the three important forms of myopathies that exist. The response to this condition varies from person to person depending on the strength and dexterity of the muscle tissue. Polymyositis is generally not localized and hence many muscle groups are affected by it.

The most common muscle groups affected by this disease are the muscles associated with the neck (sternocleido mastoid), shoulders (scapular region), trapezoid region, hands and legs mainly hams and quadriceps during walking and running. The symptoms of polymyositis are usually self-limiting. However in case of adverse muscular inflammation, medical attention is required in order to prevent progressive damage of the muscle tissue.

Clinical manifestations of Polymyositis

Polymyositis has many causes - some of the common causes include infections (bacterial or viral), and inherited forms. Viral myagias are one of the forms, which can affect the muscle tissues in an intense manner if ignored. The appropriate intervention for viral Myalgia causing Polymyositis is to identify the exact cause in ruling out other infective forms such as bacterial infection through laboratory diagnosis.

Viral particles can induce the onset of fever causing muscular weakness and fatigue. Sometimes, polymyositis can affect children under these scenarios. Other generalized clinical manifestations of the disease include low-grade fever, weakness, irritability, tenderness, decreased appetite and shortness of breath. Some forms of polymyositis have long-term effects and hence such patients are advised to incorporate immunosuppressive agents. This is recommended when Polymyositis takes the autoimmune disease form.

Diagnosis of Polymyositis

Polymyositis is predominantly diagnosed by the determination of biochemical values such as creatine kinase in the blood. Creatine kinase is produced in case of muscle cell damage, the estimation of which determines the extent of muscle damage caused. Electromyograph (EMG) is also recommended to understand the neuromuscular physiology and the disorders associated with them such as myogenic condition. This is identified by the neuromuscular electrical conduction studies.

In some cases, biopsy is recommended to understand the pathophysiology of the disease through histological anomalies. The specimen is usually taken from the quadriceps or shoulders (deltoid). The pathological identification includes the presence of infiltrated muscle cells and focal regions of muscular degeneration in the muscle fibers.

Treatment of Polymyositis

Polymyositis is predominantly treated by the administration of corticosteroids in order to reduce the inflammation. These drugs can be either given by oral route or through IV administration. Other forms of treatment include immunosuppressant administration in case of autoimmune form of the disease. Azathioprine and methotexrate are generally given as immune suppressants. Appropriate intervention through corticosteroids or immune suppressants can facilitate the motor recovery in neuromuscular conduction.