Pulmonary hypertension and right ventricular failure. Part V. Classification and pathomorphology of primary pulmonary arterial hypertension

被引:0
作者
Batyraliev, T. A. [1 ]
Makhmutkhodzhaev, S. A.
Ecinci, E.
Pataraya, S. A.
Pershukov, I. V.
Sidorenko, B. A.
Preobrazhensky, D. V.
机构
[1] Sani Konukoglu Med Ctr, Gaziantep, Turkey
[2] Presidential Med Ctr Russia, Moscow 121356, Russia
关键词
pulmonary hypertension; Venice clinical classification; idiopathic pulmonary arterial hypertension; congenital systemic-to-pulmonary shunts; anorexigens; pulmonary veno-oocclusive disease; pulmonary capillary hemangiomatosis;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In a series of articles the authors discuss literature data concerning epidemiology of pulmonary hypertension (PH), its modern classification; peculiarities of its pathogenesis and treatment in various diseases and conditions. In the sixth communication they present classification of PH accepted at the Third World PH Symposium (Venice, Italy, 2003). This classification abandons terms "primary" and "secondary" PH. Primary PH which is now recommended to be called "idiopathic pulmonary arterial hypertension" is grouped in one category with familial cases of PH, PH associated with administration of anorexigens, collagen vascular disease, congenital systemic to pulmonary shunts, portal hypertension and hyperthyroidism, as well as with pulmonary veno-oocclusive disease and pulmonary capillary hemangiomatosis, taking into consideration similarity of histopathological changes of vascular tree, pathophysiology and therapeutic approaches in these forms of PH.
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页码:75 / 81
页数:7
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