Adir Yochai, Elia Davide, Harari Sergio
Pulmonary Division, Carmel Medical Center, Faculty of Medicine, Technion, Institute of Technology, Haifa, Israel
U.O. di Pneumologia e Terapia Semi-Intensiva, Servizio di Fisiopatologia Respiratoria ed Emodinamica Polmonare, Ospedale San Giuseppe, MultiMedica IRCSS, Milan, Italy.
Eur Respir Rev. 2015 Sep;24(137):400-10. doi: 10.1183/16000617.0041-2015.
Pulmonary hypertension (PH) is a major complication of several haematological disorders. Chronic myeloproliferative diseases (CMPDs) associated with pulmonary hypertension have been included in group five of the clinical classification for pulmonary hypertension, corresponding to pulmonary hypertension for which the aetiology is unclear and/or multifactorial. The aim of this review is to discuss the epidemiology, pathogenic mechanism and treatment approaches of the more common forms of pulmonary hypertension in the context of CMPD's: chronic thromboembolic pulmonary hypertension, precapillary pulmonary hypertension and drug-induced PH.
肺动脉高压(PH)是几种血液系统疾病的主要并发症。与肺动脉高压相关的慢性骨髓增殖性疾病(CMPDs)已被纳入肺动脉高压临床分类的第五组,这一组对应的是病因不明和/或多因素的肺动脉高压。本综述的目的是在慢性骨髓增殖性疾病的背景下,讨论肺动脉高压更常见形式的流行病学、发病机制和治疗方法:慢性血栓栓塞性肺动脉高压、毛细血管前性肺动脉高压和药物性肺动脉高压。