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Silent Pulmonary Artery Dissection in a patient with old Pulmonary Balloon Valvuloplasty.一位曾接受肺动脉球囊瓣膜成形术的患者发生了无症状性肺动脉夹层。
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本文引用的文献

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Pulmonary artery dissection associated with multiple coronary-pulmonary artery fistulae.肺动脉夹层伴多发冠状动脉-肺动脉瘘
Interact Cardiovasc Thorac Surg. 2010 Aug;11(2):207-8. doi: 10.1510/icvts.2010.233841. Epub 2010 May 3.
2
PDA with Eisenmenger complicated by pulmonary artery dissection.动脉导管未闭合并艾森曼格综合征并肺动脉夹层。
Eur J Echocardiogr. 2010 Sep;11(8):E32. doi: 10.1093/ejechocard/jeq054. Epub 2010 Apr 26.
3
An unusual presentation of pulmonary artery dissection.
Thorax. 2009 Apr;64(4):368. doi: 10.1136/thx.2008.101105.
4
Pulmonary-artery dissection in patients with Eisenmenger's syndrome.艾森曼格综合征患者的肺动脉夹层
N Engl J Med. 2007 May 17;356(20):2110-2. doi: 10.1056/NEJMc063492.
5
Eisenmenger syndrome complicated by pulmonary artery dissection.艾森曼格综合征合并肺动脉夹层。
Eur Heart J. 2007 Feb;28(3):298. doi: 10.1093/eurheartj/ehl224. Epub 2006 Sep 22.
6
Pulmonary artery dissection: a rare complication of pulmonary balloon valvuloplasty diagnosed 11 years after the procedure.肺动脉夹层:一种在肺动脉球囊瓣膜成形术后11年才被诊断出的罕见并发症。
J Am Soc Echocardiogr. 2006 Sep;19(9):1191.e5-8. doi: 10.1016/j.echo.2006.05.004.
7
Endovascular treatment of concomitant patent ductus arteriosus and type B aortic dissection in a patient with pulmonary artery dissection.肺动脉夹层患者合并动脉导管未闭及B型主动脉夹层的血管内治疗
J Thorac Cardiovasc Surg. 2006 Aug;132(2):438-40. doi: 10.1016/j.jtcvs.2006.04.013.
8
Pulmonary artery dissection: an emerging cardiovascular complication in surviving patients with chronic pulmonary hypertension.肺动脉夹层:慢性肺动脉高压存活患者中一种新出现的心血管并发症。
Heart. 2005 Feb;91(2):142-5. doi: 10.1136/hrt.2004.045799.
9
Pulmonary artery dissection in patients without underlying pulmonary hypertension.无基础肺动脉高压患者的肺动脉夹层
Histopathology. 2001 May;38(5):435-42. doi: 10.1046/j.1365-2559.2001.01129.x.

一位百岁老人的无症状肺动脉夹层。

Silent pulmonary artery dissection in a centenarian.

作者信息

Matsumoto Asumi, Kawasaki Tatsuya, Takeoka Mayumi, Yamano Michiyo, Sakai Chieko, Harimoto Kuniyasu, Miki Shigeyuki, Kamitani Tadaaki

机构信息

Department of Cardiology, Matsushita Memorial Hospital, Osaka, Japan.

Department of Clinical Physiology, Matsushita Memorial Hospital, Osaka, Japan.

出版信息

J Cardiol Cases. 2011 Dec 6;5(1):e36-e38. doi: 10.1016/j.jccase.2011.10.005. eCollection 2012 Feb.

DOI:10.1016/j.jccase.2011.10.005
PMID:30532898
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6265393/
Abstract

Pulmonary artery dissection is an extremely rare and fatal disease that is difficult to diagnose. We report a case of a 97-year-old woman with heart failure, who was diagnosed as having silent pulmonary artery dissection by chance during transthoracic echocardiography. Surgical treatment for pulmonary artery dissection was not performed, but the patient has been doing well in a sanatorium for more than 2 years, being a centenarian.

摘要

肺动脉夹层是一种极其罕见且致命的疾病,难以诊断。我们报告一例97岁心力衰竭女性患者,其在经胸超声心动图检查时偶然被诊断为无症状性肺动脉夹层。未对该肺动脉夹层患者进行手术治疗,但患者在疗养院状况良好已超过2年,有望成为百岁老人。