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严重肺动脉高压的一种罕见病因:主动脉瘤压迫肺动脉及血栓形成

An Unusual Cause of Severe Pulmonary Hypertension: Compression of Pulmonary Arteries by Aortic Aneurysm and Thrombus Formation.

作者信息

Warsame Ramla, Ofuya Ruth, Thillai Ruju Smirtha, Gollapinni Uday, Kupoluyi Olufunbi, Malik Ahmed Malik Abuelgasim, Sultana Sadia

机构信息

Acute Internal Medicine, University Hospital of North Midland, Royal Stoke University Hospital, Stoke-on-Trent, GBR.

Acute Medicine, University Hospital of North Midland, Royal Stoke University Hospital, Stoke-on-Trent, GBR.

出版信息

Cureus. 2025 Aug 21;17(8):e90653. doi: 10.7759/cureus.90653. eCollection 2025 Aug.

DOI:10.7759/cureus.90653
PMID:40979020
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12449776/
Abstract

Pulmonary hypertension (PHTN) has a broad differential, ranging from common aetiologies like thromboembolism, chronic lung disease, and heart failure. External compression of the pulmonary arteries by thoracic aortic aneurysms (TAAs) is an exceptionally rare cause of PH but may significantly impact haemodynamics. We report the case of an 81-year-old woman presenting with progressive dyspnoea and peripheral oedema, who was found to have near-complete compression of the right main pulmonary artery (RMPA) by an ascending aortic aneurysm, along with intraluminal thrombus. Transthoracic echocardiography revealed severe PH with preserved left ventricular (LV) function. CT pulmonary angiography was carried out, confirming both mechanical compression of RMPA and thrombus formation. According to the existing literature, we proposed that compression-induced stasis likely contributed to thrombosis, aligning with Virchow's triad. Given the patient's frailty and comorbidities, she was managed conservatively. The multifactorial nature of this case prompts us to consider broader differentials in unexplained PH. It also acknowledges the challenges in managing larger symptomatic aneurysms in the elderly population.

摘要

肺动脉高压(PHTN)的鉴别诊断范围广泛,包括血栓栓塞、慢性肺部疾病和心力衰竭等常见病因。胸主动脉瘤(TAA)对肺动脉的外部压迫是一种极为罕见的肺动脉高压病因,但可能对血流动力学产生重大影响。我们报告了一例81岁女性病例,该患者表现为进行性呼吸困难和外周水肿,经检查发现升主动脉瘤几乎完全压迫右主肺动脉(RMPA),同时伴有腔内血栓形成。经胸超声心动图显示严重肺动脉高压,左心室(LV)功能保留。进行了CT肺动脉造影,证实了RMPA的机械性压迫和血栓形成。根据现有文献,我们认为压迫引起的血流淤滞可能导致了血栓形成,这与维勒布兰德氏三联征相符。鉴于患者身体虚弱且合并多种疾病,对其进行了保守治疗。该病例的多因素性质促使我们在不明原因的肺动脉高压中考虑更广泛的鉴别诊断。它也认识到在老年人群中处理较大的有症状动脉瘤所面临的挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0931/12449776/7b4f8ec54e9e/cureus-0017-00000090653-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0931/12449776/dcf8ea9c623e/cureus-0017-00000090653-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0931/12449776/7b4f8ec54e9e/cureus-0017-00000090653-i02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0931/12449776/dcf8ea9c623e/cureus-0017-00000090653-i01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0931/12449776/7b4f8ec54e9e/cureus-0017-00000090653-i02.jpg

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