孤立性肺动脉血管炎

IF 0.1 Q4 RESPIRATORY SYSTEM
M. Ağca, B. Yıldızeli, E. Bozkurtlar, S. Yavuz, T. Sevim
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引用次数: 0

摘要

我们报告了一例26岁女性的独特病例,该病例最初评估为肉瘤或血栓栓塞事件,其与肺动脉的临床和放射学相似,但在组织病理学检查的帮助下,在动脉内膜切除术后诊断为孤立的肺动脉血管炎。动脉内膜切除术后,可能导致血管炎的其他原因已被排除。患者在手术后接受了免疫抑制治疗,她的对照计算机断层扫描显示肺动脉管腔大开。当检测到肺动脉充盈缺陷而没有其他全身性发现时,必须将孤立性肺动脉血管炎视为鉴别诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Isolated pulmonary artery vasculitis
We present a unique case of a 26-year-old woman, which first evaluated as sarcoma or thromboembolic events with their clinical and radiological similarities of the pulmonary artery but diagnosed as isolated pulmonary artery vasculitis after endarterectomy with the help of histopathological examinations. After the endarterectomy procedure, the other causes that may lead to vasculitis had been excluded. The patient had the immunosuppressive therapy after the procedure, and her control computerized tomography revealed that the lumen of the pulmonary artery was wide open. Isolated pulmonary artery vasculitis must be considered as a differential diagnosis when a filling defect of the pulmonary artery had been detected without other systemic findings.
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来源期刊
Eurasian Journal of Pulmonology
Eurasian Journal of Pulmonology RESPIRATORY SYSTEM-
自引率
0.00%
发文量
9
审稿时长
16 weeks
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