Severe restrictive lung disease in systemic sclerosis
نویسندگان
چکیده
منابع مشابه
Association between atherosclerosis and parenchymal lung involvement in systemic sclerosis
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...
متن کاملImaging Lung Disease in Systemic Sclerosis
Interstitial lung disease and pulmonary hypertension (PH) are the most common cardiopulmonary findings in patients with systemic sclerosis (SSc). About two thirds of patients suffering from SSc develop scleroderma interstitial lung disease. PH is present in about 20% of SSc patients and is typically associated with severe lung disease, although it may be an isolated manifestation of SSc. High-r...
متن کامل- 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...
متن کاملInterstitial lung disease in systemic sclerosis
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...
متن کاملLung Involvement In Systemic Sclerosis
Systemic sclerosis (SSc) is a multisystem connective tissue disease of unknown etiology. Similar to other connective tissue diseases, SSc follows a chronic course, occurs more commonly in women, and is highly heterogeneous in its protean clinical manifestations. The hallmarks of SSc are autoimmunity and inflammation, functional and structural abnormalities in small blood vessels in multiple vas...
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ژورنال
عنوان ژورنال: Arthritis & Rheumatism
سال: 1994
ISSN: 0004-3591,1529-0131
DOI: 10.1002/art.1780370903