AUTHOR=Gao Fuguo , Liu Rui , Sun Yi , Huang He , Zuo Siyang , Yang Chengxing , Ma Po , Li Bin , Hou Yan , Xue Qingliang 

TITLE=Case Report: High altitude, young lives: unmasking pulmonary hypertension in two unique cases

JOURNAL=Frontiers in Medicine

VOLUME=Volume 12 - 2025

YEAR=2025

URL=https://www.frontiersin.org/journals/medicine/articles/10.3389/fmed.2025.1719635

DOI=10.3389/fmed.2025.1719635

ISSN=2296-858X

ABSTRACT=BackgroundThe high-altitude environment characterized by hypobaric hypoxia can cause significant damage to the cardiovascular system, particularly vascular endothelial function, and is a significant trigger for acute and chronic mountain sickness. High-altitude pulmonary hypertension (HAPH) is a serious complication induced by prolonged exposure to high altitude, characterized by abnormally elevated pulmonary artery pressure and increased right heart load, which can progress to right heart failure and be life-threatening. This article aims to enhance clinicians’ understanding of this disease through two cases of HAPH in young males.Case descriptionCase 1 was a 21-year-old male who developed progressively worsening chest pain, shortness of breath, and amaurosis fugax after living at an altitude of 4800 meters for 4 months. Case 2 was a 20-year-old male who experienced exertional dyspnea accompanied by amaurosis fugax and a brief loss of consciousness after 18 months of residence at 4,300 meters. Both patients were previously healthy with normal cardiopulmonary function before moving to high altitude. Physical examination upon presentation revealed significant hypoxemia (oxygen saturation 80 and 82% on room air, respectively). Echocardiography in both cases clearly demonstrated right atrial and right ventricular enlargement, moderate tricuspid regurgitation, with estimated systolic pulmonary artery pressures (sPAP) as high as 55 mmHg and 56 mmHg, respectively. Chest CT confirmed right heart enlargement and main pulmonary artery dilation. After systematic evaluation excluded other etiologies, HAPH was diagnosed.DiscussionThe core pathophysiology of HAPH is hypoxia-induced pulmonary vasoconstriction and remodeling. These cases demonstrate that even for young, healthy individuals, prolonged exposure to extremely high altitudes can lead to severe pulmonary hypertension and right ventricular dysfunction. Diagnosis requires a combination of high-altitude exposure history, clinical symptoms, evidence of hypoxemia, and echocardiographic findings. The most fundamental treatment for diagnosed HAPH patients is removal from the high-altitude hypoxic environment, making early recognition and intervention crucial.ConclusionThe high-altitude environment poses a serious threat to the cardiovascular systems of susceptible individuals. For patients with a history of high-altitude residence who present with relevant symptoms, clinicians should maintain a high index of suspicion for HAPH and conduct timely screening and diagnosis to prevent adverse outcomes.