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肺动脉高压

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Prognostic Effect and Longitudinal Hemodynamic Assessment of Borderline Pulmonary Hypertension Skeletal muscle mitochondrial oxidative phosphorylation function in idiopathic pulmonary arterial hypertension: in vivo and in vitro study 2015 ESC/ERS Guidelines for the diagnosis and treatment of pulmonary hypertension: The Joint Task Force for the Diagnosis and Treatment of Pulmonary Hypertension of the European Society of Cardiology (ESC) and the European Respiratory Society (ERS): Endorsed by: Association for European Paediatric and Congenital Cardiology (AEPC), International Society for Heart and Lung Transplantation (ISHLT) Evidence-based detection of pulmonary arterial hypertension in systemic sclerosis: the DETECT study The association between body mass index and obesity with survival in pulmonary arterial hypertension Impact of age and comorbidity on risk stratification in idiopathic pulmonary arterial hypertension Clinical and genetic characteristics of pulmonary arterial hypertension in Lebanon Right ventricular stroke work correlates with outcomes in pediatric pulmonary arterial hypertension Sildenafil for improving outcomes in patients with corrected valvular heart disease and persistent pulmonary hypertension: a multicenter, double-blind, randomized clinical trial 中国肺高血压诊断和治疗指南2018
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Clinical Case StudyAvailable online 23 April 2020

JOURNAL：Can J Cardiol. Article Link

Pulmonary Hypertension Caused by a Coconut Left Atrium

EC Leung, N Hirani et al. Keywords: pulmonary hypertention; coconut left atrium; chest x-ray image

ABSTRACT

“Coconut atrium” was first described in 1898 and is most commonly associated with rheumatic heart disease. This case demonstrates a dramatic chest x-ray image of extensive circumferential calcification of the left atrium. The abnormality was thought to result in elevated pulmonary pressures and severe right heart failure in the absence of significant mitral valve dysfunction.
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