Pulmonary hypertension in interstitial lung disease

被引：16
|
作者：
Nathan, S. D. [1 ]
机构：
[1] Inova Fairfax Hosp, Adv Lung Dis & Transplant Program, Inova Heart & Vasc Inst, Falls Church, VA 22042 USA
来源：
INTERNATIONAL JOURNAL OF CLINICAL PRACTICE | 2008年 / 62卷
关键词：
D O I：
10.1111/j.1742-1241.2008.01624.x
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
Pulmonary hypertension (PH) may complicate the course of many forms of advanced interstitial lung disease (ILD) and has been shown to portend a worse outcome. The aetiology of PH is likely multifactorial with variable contribution of factors amongst the different diseases. The most common such conditions include idiopathic pulmonary fibrosis, sarcoidosis, connective tissue disease-related ILD and pulmonary langerhans cell histiocytosis. Whether the course and impact of PH in these conditions can be modified by therapy requires further study.
引用
收藏
页码：21 / 28
页数：8
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