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获得性外周肺动脉瘤:疾病的形态学谱和多排螺旋 CT 血管造影表现——病例系列及文献复习。

Acquired peripheral pulmonary artery aneurysms: morphological spectrum of disease and multidetector computed tomography angiography findings-cases series and literature review.

机构信息

Department of Diagnostic Imaging, Section of General Radiology, Azienda Ospedali dei Colli, P.O. Monaldi, Via Leonardo Bianchi, 80131, Naples, Italy.

Department of Radiology, The James Cook University Hospital NHS Trust, Marton Road, Middlesbrough, TS4 3BW, UK.

出版信息

Radiol Med. 2018 Sep;123(9):664-675. doi: 10.1007/s11547-018-0900-9. Epub 2018 May 2.

Abstract

BACKGROUND

Acquired peripheral or intraparenchymal pulmonary artery aneurysms (PPAA) are rare entities but are important to recognize because of the associated morbidity. Hemoptysis is their principal complication and is a potentially fatal condition.

PURPOSE

To illustrate the causes, multidetector CT angiography (MDCTA) findings and differential diagnosis of acquired PPAA.

MATERIALS AND METHODS

The institutional review boards approved this study. We conducted a retrospective review of the demographic data and the results of clinical and laboratory examinations, and imaging studies of patients managed between January 2012 and January 2017 in two institutions.

RESULTS

A total of 19 patients had acquired PPAA that were detected at MDCTA, 9 patients with normal pulmonary artery pressures and 10 with pulmonary hypertension. Nine patients developed PPAA-related acute symptoms. MDCTA features of PPAA include: a lobulated vascular mass, an indistinct irregular arterial wall, aneurysmal thrombosis or wall calcification, findings of impending rupture including perianeurysmal edema, gas or a soft tissue mass.

CONCLUSION

PPAA are rare. In our series, endocarditis and pulmonary hypertension are the PPAA leading causes. The treatment modality preferred is embolization, especially as surgery poses a very high risk for patients with severe pulmonary hypertension. Further clarification of the natural history of these rare arterial aneurysms is needed.

摘要

背景

获得性肺外周或肺实质内动脉动脉瘤(PPAA)较为罕见,但因其相关发病率而需要被识别。咯血是其主要并发症,也是一种潜在的致命情况。

目的

阐述获得性 PPAA 的病因、多排 CT 血管造影(MDCTA)表现和鉴别诊断。

材料与方法

本研究获得了机构审查委员会的批准。我们对 2012 年 1 月至 2017 年 1 月在两家机构就诊的患者的人口统计学数据和临床及实验室检查结果以及影像学研究结果进行了回顾性分析。

结果

共 19 例患者在 MDCTA 上发现获得性 PPAA,其中 9 例肺动脉压正常,10 例患有肺动脉高压。9 例患者出现与 PPAA 相关的急性症状。PPAA 的 MDCTA 特征包括:分叶状血管肿块、动脉壁不清晰的不规则、动脉瘤血栓形成或壁钙化、提示即将破裂的征象包括动脉瘤周围水肿、气体或软组织肿块。

结论

PPAA 较为罕见。在我们的研究中,心内膜炎和肺动脉高压是导致 PPAA 的主要原因。首选的治疗方式是栓塞,特别是对于患有严重肺动脉高压的患者,手术风险非常高。需要进一步阐明这些罕见的动脉动脉瘤的自然史。

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