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肺动脉假性动脉瘤:临床特征与CT表现

Pulmonary Artery Pseudoaneurysms: Clinical Features and CT Findings.

作者信息

Chen Ying, Gilman Matthew D, Humphrey Kathryn L, Salazar Gloria M, Sharma Amita, Muniappan Ashok, Shepard Jo-Anne O, Wu Carol C

机构信息

1 Department of Radiology, Massachusetts General Hospital, Boston, MA.

2 Department of Breast Imaging and Intervention, Spectrum Health, Grand Rapids, MI.

出版信息

AJR Am J Roentgenol. 2017 Jan;208(1):84-91. doi: 10.2214/AJR.16.16312. Epub 2016 Sep 22.

Abstract

OBJECTIVE

The purpose of this study was to analyze the clinical and CT features of pulmonary artery pseudoaneurysms (PAPs).

MATERIALS AND METHODS

A database search of chest CT examinations performed from January 1, 2000 to December 31, 2014 identified 24 patients with findings consistent with PAPs. A CT finding consistent with a PAP was defined as a focal saccular outpouching of a pulmonary artery. Medical records were reviewed to determine clinical presentations, treatments, and outcomes. CT scans were reviewed by two board-certified fellowship-trained chest radiologists.

RESULTS

A total of 35 PAPs were identified in 24 patients. Hemoptysis and shortness of breath were the most common presenting symptoms. The most commonly identified causes of PAPs were infection (33%), neoplasms (13%), and trauma (17%). Of the 35 PAPs, 29 (83%) were located in segmental or subsegmental pulmonary arteries. A solitary PAP was identified in 20 (83%) patients, and multiple PAPs were identified in three patients with endocarditis and one patient with pulmonary metastases. Only three of 35 (9%) PAPs were associated with a ground-glass halo. Endovascular treatment was successfully performed in 12 patients, and only one patient had immediate recurrent hemoptysis after treatment. PAP was clinically suspected by the referring clinicians in only three patients. Sixteen of the 35 (46%) PAPs were not reported on the initial CT studies.

CONCLUSION

PAPs showed a strong predilection for the peripheral pulmonary arteries. Multiplicity of PAPs can be seen in the settings of endocarditis and pulmonary metastatic disease. Most PAPs were not associated with a ground-glass halo. PAPs can be lethal but were often not suspected clinically and were underreported by radiologists.

摘要

目的

本研究旨在分析肺动脉假性动脉瘤(PAPs)的临床及CT特征。

材料与方法

对2000年1月1日至2014年12月31日期间进行的胸部CT检查数据库进行检索,确定了24例具有与PAPs相符表现的患者。与PAPs相符的CT表现定义为肺动脉的局灶性囊状膨出。查阅病历以确定临床表现、治疗方法及预后。由两位经过胸科放射学专科培训并获得委员会认证的放射科医生对CT扫描进行评估。

结果

24例患者中共发现35个PAPs。咯血和呼吸急促是最常见的首发症状。PAPs最常见的病因是感染(33%)、肿瘤(13%)和创伤(17%)。在35个PAPs中,29个(83%)位于段或亚段肺动脉。20例(83%)患者发现单个PAPs,3例感染性心内膜炎患者和1例肺转移患者发现多个PAPs。35个PAPs中只有3个(9%)与磨玻璃晕征相关。12例患者成功进行了血管内治疗,只有1例患者治疗后立即出现反复咯血。转诊医生仅在3例患者中临床怀疑有PAPs。35个PAPs中有16个(46%)在初始CT检查中未被报告。

结论

PAPs强烈倾向于发生在肺外周动脉。在感染性心内膜炎和肺转移性疾病中可出现多个PAPs。大多数PAPs与磨玻璃晕征无关。PAPs可能致命,但临床上常未被怀疑,放射科医生报告也较少。

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