Scleroderma

January 31, 2006There are a lot of infirmitys today, some distempers we manage a lot about and are curable others are non; then in that respect are the disorders we just sire?t know a lot about and rush no redress. Scleroderma is a disease that we know a miniature bit about but construct to cure. patient role and their families that do encounter the disease gain questions. Questions like what is Scleroderma, we know at that place is no cure but is there cherish manpowert for it, and what is the outlook?The word genus Scleroderma comes from deuce Greek words: ?sclero? convey hard, and ?derma? meaning tegument. Scleroderma is an autoimmune disease of the connecter tissue. It is a chronic disease. ?Scleroderma is characterized by the nervous straination of bread tissue (fibrosis) in the clamber and organs of the body.?(Medifocus, 2006) This leads to thickness and solution of involved areas. Scleroderma is in like modal value referred to as systemic sclerosis. The construct of Scleroderma is unknown. Fortunately, scleroderma is relatively uncommon affecting around 300,000 persons in the United States. The dis place most commonly f every(prenominal)s in women between the ages of twenty and forty; however men and children lavatory be stirred as well. The disease is not hereditary and is not pattern to be inherited. There are two categories of Scleroderma disperse and limited. The diffuse form of scleroderma is involves proportionate thickening of skin of the extremities, face, trunk (chest, back, and abdomen) which can rapidly girdment to hardening afterwards an early inflammatory phase. Organ disease can drop dead early on and be serious. organs affected imply the esophagus, bowels, lungs (with scarring), heart, and kidneys. The limited form of scleroderma tends to be toward the skin of the fingers and face. The skin changes and other features of disease tend to occur more belatedly than in the diffuse form. ?The diagn osis of the scleroderma syndrome is based on! the finding of the clinical features of the illnesses. Nearly exclusively patients with scleroderma have blood tests which suggest autoimmunity, antinuclear antibodies (ANAs). A event antibody, the anticentromere antibody, is found or so exclusively in the limited form of scleroderma. Anti-Scl 70 antibody (antitopoisomerase I antibody) is most often seen in patients with the diffuse form of scleroderma.? (Medicine Net. Inc., 2006) former(a) tests are employ to quantify the front of any informal disease. These may accommodate upper and cut back GI tests to evaluate the bowels, chest x-rays, and lung function tests to examine the lungs, electrocardiogram and echocardiograms to evaluate the heart and lung arteries. Currently there is no cure for Scleroderma. thus far though there are no cures for the disease (or syndrome) there are treatment options. The treatment options depend on the location, or if it is diffused or limited. In general, medications that may be used incl ude immunosuppressive agents, antifibrotic agents, anti-inflammatory agents, vasodilators, and angiotensin-converting enzyme inhibitors (Medifocus, 2006). In rare cases, when symptoms of systemic sclerosis become severe, surgery may be recommended.

The outlook varies for patients depending on which caseful of scleroderma they have. Scientist swears that it is often unenviable to cod a prognosis in the early stages of the disease. Scientist also say that the prognosis for patients with limited sclerosis who do not maturate pulmonary hypertension is good; but men who develop the disease, patients with diffuse scleroderma, and patients who experience kidney, lung, and heart involvement m! ainly have a worse prognosis. ReferencesMedifocus, (2006). Scleroderma. Retrieved January 7, 2007, from Scleroderma guide contain Website: hypertext take away protocol://www.scleroderma-info.com/guide_detail.aspMedicine Net, (2006). Scleroderma, symptom and treatments. Retrieved January 7, 2007, fromScleroderma cancer Web site: http://www.medicinenet.com/scleroderma/index.htmKleinert, S., Tony, H.P., & Kneitz, C. (Oct 2006)Systemic sclerosis./SystemischeSklerose. In Der Internist, 47, p1051(12). Retrieved January 8, 2007, from HealthReference Center Academic via Thomson Gale: http://find.galegroup.com/itx/infomark.do?&contentSet=IACDocuments&type=retrieve&tabID Its all on the net for any sensation to google, whats the value appendix in this essay? Please make an effort to include any practical experiences in diagnosis or treatment. If you expect to get a full essay, order it on our website: BestEssayCheap.com

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