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The following is information about Systemic Lupus Erythematosus.

The author is Mark Flanigan.

1.0 Definition:

Systemic Lupus Erythematosus, or SLE, is a disorder of the immune system which is referred to
as an autoimmune disease. In this condition, the body’s immune system reacts against its own
cells leading to the deposition of immune complexes in tissues of various parts of the body.
It affects multiple tissues and organs of the body by causing cell damage and inflammation and
subsequent tissue damage. Systemic refers to its ability to affect almost any part of the body.
Lupus is Latin for wolf, so named over 100 years ago by a doctor who thought the rash on the
face looked like a wolf bite. And the final word, Erythematosus, refers to a reddening of the
skin.

The condition can affect anyone, but is found primarily (approximately 90 percent of cases) in
women of child-bearing age. It is also found more commonly amongst certain ethnic groups,
including blacks, Hispanics and Asians. It is a relatively rare disease, affecting between 15
to 50 in 100,000 of the population.

Other diseases that are autoimmune include Multiple Sclerosis (MS), Hashimoto's Thyroiditis,
Idiopathic Thrombocytopenic Purpura (ITP), Rheumatoid Arthritis, Type 1 Diabetes which is also
Insulin Dependent Diabetes Mellitis, and several others.

2.0 Causes

Despite much research, the disease still remains of unknown aetiology. It is believed, however,
that the condition may be triggered by infection of a pathogen that resembles some of the
body’s own proteins. When the immune system is triggered to eliminate the pathogen, it also
mistakenly identifies some of its proteins as being foreign also, and develops antibodies to
them. Another line of belief suggests that the disease occurs when the immune system becomes
overactive, as in the case of a severe infection, and then does not reduce its intensity after
the infection has been brought under control. A normal immune system will turn down its
activity after the infection has passed, but it appears that this is not the case with SLE.
In both situations the resultant reaction within the body leads to immune complexes being
deposited around various areas and different systems of the body. This will vary according to
a combination of hormonal factors, genetics, previous exposures the immune system has reacted
to, and perhaps other factors that have not yet been determined. Because these factors vary
vastly between individuals, so too do the symptoms, pattern of formation and clinical
expression of the disease.

3.0 Clinical manifestations

(signs, symptoms, description of anatomical and physiological changes that cause the clinical
manifestations)

Signs and symptoms of SLE vary widely between individuals, with some experiencing symptoms in
only one area of the body. Others can experience a variety of symptoms affecting multiple
organs or systems. Some common characteristics of SLE include the following:
- Red skin rashes, particularly in the shape of a butterfly, on the face, also after exposure
to the sun.
- Arthritic type pain in the joints as a result of inflammation, ranging from mild to severe
pain. Long term inflammation can result in permanent damage to the joint and surrounding tissue.
- Conditions affecting the CNS, including headaches, mild cognitive dysfunction and seizures
due to areas of the brain and spinal cord being affected.
- Lateral chest pain, particularly upon deep breathing, due to inflammation of the lungs, or
inflammation of the chest cavity.
- Medial chest pain due to inflammation of the heart itself or the membrane surrounding it.
- Fever of unknown origin (immune reaction).
- Glomerulonephritis, or inflammation of the kidney, most often requiring a urine or blood
test analysis for diagnosis. This can be critical, as it may lead to dangerously high blood
pressure, kidney failure, and ultimately death. The symptoms leading to kidney failure are
often very subtle so may remain undetected.
- Ulcers in the mouth and nose.
- Restricted circulation to the extremities due to inflamed blood vessels.
- Other blood conditions, including anemia, leukopenia, thrombocytopenia and blood clots,
due to antibodies against red and white blood cells.
- Weight loss.
- Swollen glands.
- Extreme fatigue.
- Muscle aches.
4.0 Risk factors
There are a number of risk factors that may be involved. These include exposure to ultra violet
radiation, genetic pre-disposition, gender - as females are more likely to incur the disease
than males, and exposure to unknown environmental factors. Certain drugs also induce lupus
like symptoms, but these usually abate when the drug use is discontinued.
5.0 Diagnostic techniques
The system of differential diagnosis is used to determine whether a patient has SLE. Accurate
diagnosis is not easy, due to the enormous variation in symptoms and lack of a specific
indicator. In order for a patient to be diagnosed, they must have at least 4 of the common
criteria, most of which are listed under clinical manifestations.
Renal biopsy is often performed to determine degree of kidney damage.
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