The heart and pulmonary vasculature in scleroderma: clinical features and pathobiology

被引:44
作者
Coghlan, JG [1 ]
Mukerjee, D [1 ]
机构
[1] Royal Free Hosp NHS Trust, Dept Cardiol, London NW3 2QG, England
关键词
D O I
10.1097/00002281-200111000-00008
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
For nearly 50 years there have been concerns that scleroderma affects the heart. The two main mechanisms that are thought to be involved are; a fibrotic process secondary to myocardial Raynaud phenomenon (RP) or an immune-mediated myocarditis, In the past year several studies have been published that confirm the frequent occurrence of subclinical cardiac abnormalities in scleroderma. These studies do not tend to support the myocardial RP theory and raise doubts about the prognostic significance of these minor abnormalities. Involvement of the lungs in the form of pulmonary hypertension affects between 7-50% of patients with scleroderma. Until the past year this has been regarded by most as an untreatable condition associated with an inexorable decline. Epoprostenol therapy has now been proven beneficial in a randomized clinical trial, and several other agents show promise in the treatment of this condition. Furthermore, it is becoming apparent that lung transplantation is as successful in patients with scleroderma, as it is in primary pulmonary hypertension Curr Opin Rheumatol 2001, 13:495-499 (C) 2001 Lippincott Williams & Wilkins, Inc.
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收藏
页码:495 / 499
页数:5
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