Lung Function and Survival in Systemic Sclerosis Interstitial Lung Disease
نویسندگان
چکیده
منابع مشابه
- Cerinic Interstitial lung disease in systemic sclerosis
Lung involvement frequently complicates systemic sclerosis (SSc), provoking loss of quality of life and a poor expectation of survival. For this reason an early diagnosis of lung involvement is warranted: high-resolution computed tomography (HRCT), pulmonary function tests (PFT), lung scintigraphy with DTPA and bronchoalveolar lavage (BAL) are mandatory to define and follow-up pulmonary interst...
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Systemic sclerosis (SSc) is a connective tissue disease characterised by autoimmune features, widespread vasculopathy and fibrosis of the skin and internal organs. The pattern of internal organ involvement and the natural history of the disease are highly variable. Although the etiology is unknown, most studies point to links between genetic predisposition and environmental factors. SSc has bee...
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Background: Systemic sclerosis is an autoimmune disease affecting connective tissues, (including epidermal, subepidermal, microvasculature, etc.), leading to various extent of end-organ damage. The leading cause of mortality among these patients is lung involvement. The cardiovascular events happen more frequently in patients suffering systemic scleroderma, comparing to healthy population. This...
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Interstitial lung disease (ILD) is common in systemic sclerosis (SSc) patients and despite recent advances in the treatment is, at present, the major cause of death. Today, an early diagnosis of ILD is possible, and is mandatory to improve the prognosis of the disease. Pulmonary function tests and high-resolution computed tomography remain the mainstay for the diagnosis of SSc-ILD, but there is...
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ژورنال
عنوان ژورنال: The Journal of Rheumatology
سال: 2014
ISSN: 0315-162X,1499-2752
DOI: 10.3899/jrheum.140156