Scleroderma natural history, complications and prognosis: Difference between revisions

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Revision as of 01:20, 6 February 2018

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

@@ Line 6: / Line 6: @@
 ==Natural History==
 ==Complications==
-Diffuse scleroderma can cause [[musculoskeletal system|musculoskeletal]], [[lung|pulmonary]], [[gastrointestinal tract|gastrointestinal]], [[kidney|renal]] and other complications. Patients with larger amounts of cutaneous involvement are more likely to have involvement of the internal tissues and organs.
-The most common cause of death in people with scleroderma is scarring of the lungs, called [[pulmonary fibrosis]].
-Other complications of scleroderma include:
-* [[Cancer]]
-* [[Heart failure]]
-* High blood pressure in the lungs ([[pulmonary hypertension]])
-* [[Kidney failure]]
-* Problems absorbing nutrients from food ([[malabsorption]])
-==Prognosis==
-Some people with scleroderma have symptoms that develop quickly over the first few years and continue to get worse. However, in most patients, the disease slowly gets worse.
-People who only have skin symptoms have a better outlook. Widespread (systemic) scleroderma can damage the heart, kidney, lungs, or GI tract, which may cause death.
-Lung problems are the most common cause of death in patients with scleroderma.
 ==References==