Pulmonary Hypertension in A Patient With Systemic Sclerosis

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Pulmonary hypertension in systemic sclerosis.

A woman born in 1912 (Case 8 in the necropsy series) had an unremarkable family history. In 1940, she first noted blanching and cyanosis of the fingers on exposure to cold. Since 1960, small, hard, subcutaneous nodules developed at different locations on her body. Early in 1968, progressive effort dypsnoea and anginal chest pains started insidiously, and treatment with digitalis, furosemide, an...

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Pulmonary hypertension in systemic sclerosis: different phenotypes.

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Pulmonary arterial hypertension in systemic sclerosis.

Pulmonary arterial hypertension (PAH) in systemic sclerosis (SSc) is a complex clinical situation resulting from restricted flow through the pulmonary arterial circulation ending in increased pulmonary vascular resistance and right heart failure. PAH is a common and life-threatening complication in connective tissue diseases, specifically in SSc if not treated rapidly and adequately. Based on t...

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Prevalence of pulmonary hypertension in systemic sclerosis.

OBJECTIVE To assess the prevalence of pulmonary arterial hypertension (PAH) in patients with the diagnosis of systemic sclerosis (SSc) followed at a tertiary university service. MATERIAL AND METHODS Fifty-seven patients with SSc were studied by clinical assessment directed at the cardiopulmonary system, pulmonary function tests and Doppler echocardiography (ECHO). The following criteria were ...

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ژورنال

عنوان ژورنال: IOSR Journal of Dental and Medical Sciences

سال: 2017

ISSN: 2279-0861,2279-0853

DOI: 10.9790/0853-1604020104