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升主动脉夹层后并发罕见的囊状动脉瘤和大肺动脉瘤伴继发性栓塞 1 例报告。

A rare case of a simultaneous post-dissection saccular aneurysm of the ascending aorta and large pulmonary artery aneurysm with secondary embolism: a case report.

机构信息

Department of Cardiothoracic Surgery, Radboud University Medical Center, Geert Grooteplein Zuid 10, Nijmegen, 6525 GA, The Netherlands.

Department of Cardiothoracic Surgery, St. Antoniushospital, Nieuwegein, The Netherlands.

出版信息

J Cardiothorac Surg. 2024 Jun 21;19(1):346. doi: 10.1186/s13019-024-02865-x.

DOI:10.1186/s13019-024-02865-x
PMID:38907334
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11191314/
Abstract

BACKGROUND

Aneurysms of the pulmonary arteries and the ascending aorta are rare, and both bear a high mortality risk if left untreated. In general, these entities are primarily caused by etiologies such as hypertension, pulmonary arterial hypertension, infection or congenital disorders. Treatment requires a rapid diagnostic work-up or even immediate surgical intervention in acute cases. Nevertheless, surgery entails serious perioperative risks, in particular in patients with multiple comorbidities.

CASE PRESENTATION

We discuss a 70-year-old woman presented with decompensated heart failure based on severe pulmonary artery hypertension, coincided by a massive pulmonary artery aneurysm with secondary embolism. Additional diagnostic imaging also showed a chronic post-dissection, saccular aneurysm of the ascending aorta. To our knowledge, this simultaneous diagnosis of a saccular aneurysm of the ascending aorta and a large aneurysm of the pulmonary artery with secondary embolism has not yet been described. Nonetheless, conservative treatment was chosen due to extensive pulmonal and cardiovascular comorbidities and the high-risk profile of surgery.

CONCLUSIONS

Extensive aneurysmatic disease of the pulmonary arteries and ascending aorta come with a serious burden of disease, especially if coincided by severe pulmonal and cardiovascular comorbidities. Both conditions can be curatively treated by surgical intervention. However, in every case the risk of surgery and the patient's vitality, comorbidities and wishes should be taken into account to formulate an adequate treatment plan. Therefore, shared decision making is of utter importance.

摘要

背景

肺动 脉和升主动 脉的动 脉瘤均较为罕见,如果不进行治疗,两者的死亡率都很高。一般而言,这些病 变主要由高血 压、肺动 脉高血 压、感染或先天 性疾 病等病因引起。治疗需要快速进行诊断检查,甚至在急性病例中需要立即进行手术干预。然而,手术会带来严重的围手术期风险,特别是对于合并多种并 发症的患者。

病例介绍

我们讨论了一位 70 岁的女性,因严重的肺动 脉高血 压导致心力衰竭失代偿,同时伴有巨大的肺动 脉瘤并继发栓 塞。进一步的影像学检查还显示升主动 脉慢性夹层后囊状动 脉瘤。据我们所知,这种升主动 脉囊状动 脉瘤和大肺动 脉瘤伴继发栓 塞的同时诊断尚未见报道。尽管如此,由于广泛的肺和心血 管并 发症以及手术的高风险,选择了保守治疗。

结论

广泛的肺动 脉和升主动 脉动 脉瘤病 变负担沉重,尤其是在伴有严重肺和心血 管并 发症时。两种情况均可通过手术干预得到治愈。然而,在每种情况下,都应考虑手术风险以及患者的活力、并 发症和意愿,以制定适当的治疗计划。因此,共同决策至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/797f/11191314/097fa6dc3837/13019_2024_2865_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/797f/11191314/863d23f1f37c/13019_2024_2865_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/797f/11191314/097fa6dc3837/13019_2024_2865_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/797f/11191314/863d23f1f37c/13019_2024_2865_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/797f/11191314/097fa6dc3837/13019_2024_2865_Fig2_HTML.jpg

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