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Survival prospects of treatment naïve patients with Eisenmenger: a systematic review of the literature and report of own experience Contemporary prevalence of pulmonary arterial hypertension in adult congenital heart disease following the updated clinical classification 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) Immunotherapy of Endothelin-1 Receptor Type A for Pulmonary Arterial Hypertension Echocardiographic Screening for Pulmonary Hypertension in Congenital Heart Disease: JACC Review Topic of the Week Factors associated with pulmonary arterial hypertension (PAH) in systemic sclerosis (SSc) Bridging the Gap Between Epigenetic and Genetic in PAH Left main coronary artery compression in pulmonary hypertension A Case of Pulmonary Hypertension Associated with Idiopathic Hypereosinophilic Syndrome Pulmonary Hypertension Caused by a Coconut Left Atrium
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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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