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重度先天性肺动脉狭窄所致肺动脉瘤。病例报告及文献综述。

Pulmonary artery aneurysm due to severe congenital pulmonic stenosis. Case report and literature review.

作者信息

Tami L F, McElderry M W

机构信息

Department of Internal Medicine, Harper Hospital, Detroit, Michigan.

出版信息

Angiology. 1994 May;45(5):383-90. doi: 10.1177/000331979404500508.

DOI:10.1177/000331979404500508
PMID:8172386
Abstract

Although dilatation of the pulmonary artery (PA) is characteristic of pulmonic valve stenosis (PVS), the occurrence of a PA aneurysm in association with PVS is very rare. The authors describe a patient with severe, dome-shaped PVS who developed a 6.5 cm pulmonary trunk aneurysm. Long-term follow-up after surgical valvotomy demonstrated that the size of the aneurysm remained unchanged. Pertinent literature and implications on the natural history and management of these aneurysms are discussed.

摘要

虽然肺动脉(PA)扩张是肺动脉瓣狭窄(PVS)的特征,但与PVS相关的PA动脉瘤的发生非常罕见。作者描述了一名患有严重圆顶状PVS的患者,该患者出现了一个6.5厘米的肺动脉干动脉瘤。手术瓣膜切开术后的长期随访表明,动脉瘤的大小保持不变。本文讨论了相关文献以及这些动脉瘤的自然病史和管理意义。

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Angiology. 1994 May;45(5):383-90. doi: 10.1177/000331979404500508.
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