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伪装为难治性肺栓塞的肺动脉肉瘤:一例报告

Pulmonary artery sarcoma masquerading as refractory pulmonary embolism: A case report.

作者信息

Yang Xinyue, Luo Jianfang, Chen Jiaohua

机构信息

Department of Cardiology, Guangdong Cardiovascular Institute, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangzhou, China.

Department of Cardiology, Guangdong Cardiovascular Institute, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Southern Medical University, Guangzhou, China.

出版信息

Sci Prog. 2025 Jan-Mar;108(1):368504251330987. doi: 10.1177/00368504251330987. Epub 2025 Mar 28.

Abstract

Pulmonary artery sarcoma (PAS) is a rare but aggressive malignancy often misdiagnosed as pulmonary embolism (PE) due to similar clinical presentations. This case report presents an early 40s female with progressive dyspnea, hemoptysis, high pulmonary arterial pressures (112 mmHg), and right heart strain unresponsive to anticoagulation therapy. Imaging findings, including cardiac magnetic resonance and positron emission tomography-computed tomography, ultimately revealed PAS. This case highlights the importance of considering rare etiologies, such as PAS, in patients with PE-like symptoms refractory to standard treatment. Early detection using advanced imaging techniques can improve diagnostic accuracy and outcomes in this rare malignancy.

摘要

肺动脉肉瘤(PAS)是一种罕见但侵袭性强的恶性肿瘤,由于临床表现相似,常被误诊为肺栓塞(PE)。本病例报告介绍了一名40岁出头的女性,她出现进行性呼吸困难、咯血、肺动脉高压(112 mmHg)以及右心劳损,对抗凝治疗无反应。包括心脏磁共振成像和正电子发射断层扫描 - 计算机断层扫描在内的影像学检查结果最终确诊为PAS。该病例强调了对于标准治疗无效的类似PE症状患者,考虑诸如PAS等罕见病因的重要性。使用先进成像技术进行早期检测可提高这种罕见恶性肿瘤的诊断准确性和治疗效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61c9/11954558/31e7d0f82354/10.1177_00368504251330987-fig1.jpg

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