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[慢性主动脉夹层对右肺动脉的压迫]

[Compression of the right pulmonary artery by chronic aortic dissection].

作者信息

Goullard L, Millaire A, Tison E, Fouquoire B, Manouvrier J, Marache P, Warembourg H, Ducloux G

机构信息

Service de cardiologie, hôpital Cardiologique, Lille.

出版信息

Arch Mal Coeur Vaiss. 1989 Apr;82(4):619-22.

PMID:2500918
Abstract

The authors report the case of a 56-year old woman who had presented with clinical symptoms resembling those of pulmonary embolism and due to chronic dissection of the first aortic segment compressing the right branch of the pulmonary artery. Eighteen months after the acute episode, the diagnosis was suspected at echocardiography, but the other paraclinical examinations performed (scintigraphy of the lung, angiography, computerized tomography) failed to display the aortic dissection, although they enabled the diagnosis to be approached and the physiopathology to be determined. At surgery, a type II dissection was discovered, the compression was relieved and the pulmonary artery was recanalized. The post-operative period was uneventful, with return to normal of the scintigraphic and CT images. This case is exceptional in that it is extremely rare (this is the 6 th case reported) and the lesion was well tolerated, probably due to the presence of a systemic-pulmonary circulation.

摘要

作者报告了一例56岁女性病例,该患者出现了类似肺栓塞的临床症状,病因是第一主动脉段慢性夹层分离压迫肺动脉右支。急性发作18个月后,超声心动图怀疑有该诊断,但所进行的其他辅助检查(肺部闪烁扫描、血管造影、计算机断层扫描)均未显示主动脉夹层分离,尽管这些检查有助于接近诊断并确定病理生理情况。手术中发现为II型夹层分离,解除了压迫,肺动脉再通。术后过程顺利,闪烁扫描和CT图像恢复正常。该病例很特殊,因为极为罕见(这是报告的第6例),而且病变耐受性良好,可能是由于存在体肺循环。

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