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白塞病患者的肺部受累:15例报告。

Pulmonary involvement in patients with Behçet's disease: report of 15 cases.

作者信息

Zhang Xiaolei, Dai Huaping, Ma Zhanhong, Yang Yuanhua, Liu Yan

机构信息

Pulmonary and Critical Care Department, Beijing Institute of Respiratory Medicine, Beijing Chao-Yang Hospital, Capital Medical University, Beijing, China.

出版信息

Clin Respir J. 2015 Oct;9(4):414-22. doi: 10.1111/crj.12153. Epub 2014 May 21.

Abstract

BACKGROUND AND OBJECTIVES

Behçet's disease (BD) is a multisystem vasculitis, and pulmonary involvement in BD can have complex clinical manifestations. We aimed to analyze the clinical and radiological features, as well as the outcomes, of BD patients with pulmonary manifestation.

METHOD

We retrospectively reviewed the medical records of 106 patients with BD diagnosed in our institute between January 2000 and January 2013. Patients with pulmonary vascular or parenchymal abnormalities on chest radiography, thorax computed tomography, magnetic resonance imaging or pulmonary scintigraphy were included in this study.

RESULTS

Fifteen patients (14%) were identified to have pulmonary involvement. Pulmonary artery aneurysms (PAA) was observed in six patients, and all of them had concomitant thrombi, attenuation or occlusion of PAs, and five of them also had radiographic parenchymal changes. Three patients had solely pulmonary artery thrombus (PAT) without PAA. For the six patients with isolated radiographic parenchyma changes, pulmonary infiltration resolved with immunosuppressant therapy in four subjects; the lesion remained unchanged in one subject with radiographic interstitial changes, and acid-fast bacilli were found in the remaining subject. Patients with PAA or PAT had more frequency of hemoptysis and extra-pulmonary vascular lesions compared with isolated parenchymal involvement. Radiographic parenchyma changes are nonspecific, with ill-defined ground-glass opacity being the most common pulmonary radiographic parenchymal changes. Patients with isolated parenchymal changes had better prognosis than those with PAA or PAT.

CONCLUSIONS

BD with pulmonary involvement can have a wide spectrum of abnormal clinical and radiographic manifestations, and multiple pulmonary lesions can exit in the same patient.

摘要

背景与目的

白塞病(BD)是一种多系统血管炎,BD的肺部受累可具有复杂的临床表现。我们旨在分析有肺部表现的BD患者的临床和放射学特征以及预后情况。

方法

我们回顾性分析了2000年1月至2013年1月在我院确诊的106例BD患者的病历。本研究纳入胸部X线、胸部计算机断层扫描、磁共振成像或肺闪烁扫描显示有肺血管或实质异常的患者。

结果

15例(14%)患者被确定有肺部受累。6例患者观察到肺动脉瘤(PAA),所有这些患者均伴有肺动脉血栓形成、肺动脉狭窄或闭塞,其中5例还伴有影像学实质改变。3例患者仅有肺动脉血栓(PAT)而无PAA。对于6例单纯有影像学实质改变的患者,4例患者经免疫抑制治疗后肺部浸润消退;1例有影像学间质改变的患者病变无变化,其余1例患者发现抗酸杆菌。与单纯实质受累相比,PAA或PAT患者咯血和肺外血管病变的发生率更高。影像学实质改变不具有特异性,边界不清的磨玻璃影是最常见的肺部影像学实质改变。单纯实质改变的患者预后优于PAA或PAT患者。

结论

有肺部受累的BD可出现广泛的异常临床和影像学表现,同一患者可存在多种肺部病变。

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