systemic lupus erythematosus.docx

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    SYSTEMIC LUPUS ERYTHEMATOSUS

    Introduction

    Systemic lupus erythematosus (SLE) is a rheumatic disease characterized by autoantibodies

    directed against self-antigens, immune complex formation, and immune dysregulation, resulting

    in damage to essentially any organ. Incidence rates among children younger than age 15 years

    have been reported to be 0.5-0.6 case per 100,000 persons. Prevalence rates of 4-250 cases per

    100,000 persons have been reported. Prevalence rates are higher in females than in males. A

    female-to-male ratio of approximately 4:1 occurs before puberty and after menopause, with a

    ratio of 8:1 between onset and loss of estrogen cycles.1

    Systemic lupus erythematosus (SLE or lupus) is a disease in which the immune system is

    overactive and does not function properly. The immune system attacks the body and creates

    inflammation in the skin, joints, kidneys, lungs, nervous system, and other organs of the body.

    People with lupus can have times of very active disease, called a flare, and times where the

    disease is mostly quiet, called remission. The specific cause of SLE is not known. It is thought to

    be a combination of multiple factors. These might include the environment (e.g., a virus, sun, or

    drug reactions), hormones (puberty), and/or a genetic predisposition to have an overactive

    immune system. Children with lupus often have one or more of symptoms like fever, fatigue,

    weight los, arthritis or joint pain"Butterfly rash" on the cheeks and bridge of the nose, or other

    rashes, sores in the mouth or nose, seizures or other nervous system problems (depression,

    psychosis), kidney problems (abnormal urine tests).2

    Lupus is a disease that is diagnosed by a combination of at least four physical symptoms

    and/or blood test abnormalities. Some of these tests measure the presence of auto-antibodies.

    Antibodies are proteins that normally help protect the body from invaders, like viruses and

    bacteria. Auto-antibodies in lupus attack normal components of cells and tissues of the body.

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    There are many successful treatments for lupus. The types of medications required will

    depend on the symptoms. Nearly all patients with lupus will require at least one medication,

    while many patients need several medications. Common medication to control disease activity is

    corticosteroid, hydroxychloroquine, immunosuppressive drugs are used to lower the immune

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    system to stop the attack. Other medications help control pain, including nonsteroidal anti-

    inflammatory drugs (NSAIDs). Because the cause of SLE is unknown, no one knows how to

    prevent it. Flares of lupus may be reduced by avoiding sun exposure (wearing strong sunscreen,

    hats, long-sleeved shirts in the sun), getting adequate sleep, and taking recommended

    medications. Risk of osteoporosis may be reduced by taking calcium and vitamin D. Systemic

    lupus erythematosus (SLE) is a high-risk disease with the possibility of end-organ damage to any

    vital or nonvital organ. This damage can severely affect organ function and can lead to decreased

    quality of life.2