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从诊断到消失:一例关于抗凝治疗房间隔血栓的病例报告

From diagnosis to disappearance: a case report on managing atrial septal thrombus with anticoagulation.

作者信息

Liu Lei, Peng Miaoxin, Fang Aijuan, Chen Hui, Yao Jing

机构信息

Department of Ultrasound Medicine, Affiliated Drum Tower Hospital of Nanjing University Medical School, No.321 Zhongshan Road, Nanjing, Jiangsu Province 210000, China.

Medical Image Center, Affiliated Drum Tower Hospital of Nanjing University Medical School, No.321 Zhongshan Road, Nanjing, Jiangsu Province 210000, China.

出版信息

Eur Heart J Case Rep. 2025 May 14;9(5):ytaf240. doi: 10.1093/ehjcr/ytaf240. eCollection 2025 May.

Abstract

BACKGROUND

The occurrence of atrial septal impending paradoxical embolism in a patent foramen ovale is a rare clinical phenomenon. In a patient with pulmonary artery embolism, transthoracic echocardiography (TTE) revealed a -atrial septal impending paradoxical embolism. This prompted us to consider: What is the nature of this cardiac lesion, and why is it embedded in the patent foramen ovale?

CASE SUMMARY

A 37-year-old man presented with chest tightness and shortness of breath for 1 week, acutely worsening in the last day before admission. Enhanced computed tomography of the pulmonary artery indicated extensive pulmonary embolism, while TTE showed a large earthworm-shaped mass (∼4.2 cm × 1.4 cm) in the atrial septal fossa ovalis, oscillating slightly with the cardiac cycle. Initially, it was unclear whether the mass was a thrombus or a myxoma. However, after 12 days of anticoagulation, the mass disappeared, suggesting it was a thrombus. The patient underwent percutaneous pulmonary thrombectomy of both arteries, resulting in symptom improvement and stabilized vital signs. Given the patient's young age, such a massive embolic event was unusual. Genetic testing for thrombophilia revealed a gene mutation, clarifying the aetiology.

DISCUSSION

Pulmonary embolism-induced pulmonary arterial hypertension increased right-to-left shunting through the atrial septal patent foramen ovale, contributing to impending paradoxical embolism development at this site. Thrombophilia might be a key risk factor for this venous thrombotic event.

摘要

背景

卵圆孔未闭时发生房间隔临近矛盾栓塞是一种罕见的临床现象。在一名肺动脉栓塞患者中,经胸超声心动图(TTE)显示存在房间隔临近矛盾栓塞。这促使我们思考:这种心脏病变的本质是什么,以及它为何嵌顿于卵圆孔未闭处?

病例摘要

一名37岁男性因胸闷、气短1周入院,入院前1天症状急性加重。肺动脉增强计算机断层扫描显示广泛的肺动脉栓塞,而TTE显示卵圆窝处有一个大的蚯蚓状肿物(约4.2 cm×1.4 cm),随心动周期轻微摆动。最初,肿物是血栓还是黏液瘤并不明确。然而,抗凝治疗12天后肿物消失,提示其为血栓。患者接受了双侧肺动脉经皮血栓切除术,症状改善,生命体征稳定。鉴于患者年轻,如此大规模的栓塞事件并不常见。血栓形成倾向的基因检测发现一种基因突变,明确了病因。

讨论

肺动脉栓塞导致的肺动脉高压增加了经卵圆孔未闭的右向左分流,促使该部位发生临近矛盾栓塞。血栓形成倾向可能是这一静脉血栓事件的关键危险因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8464/12117369/4cdfd7dfe4d4/ytaf240il2.jpg

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