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肺部细菌感染继发血管炎:一例报告

Vasculitis Secondary to Pulmonary Bacterial Infection: A Case Report.

作者信息

Zhou Wangji, Ye Wei, Shi Juhong, Ai Sanxi, Tian Xinlun

机构信息

Department of Pulmonary and Critical Care Medicine, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing 100730, China.

Department of Nephrology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing 100730, China.

出版信息

Diagnostics (Basel). 2022 Mar 22;12(4):772. doi: 10.3390/diagnostics12040772.

Abstract

Vasculitides are a heterogeneous group of primary disorders which may occur secondary to a variety of conditions. Among them, vasculitis caused by bacterial infection is rare. Here, we present images of CT scans and histology from a 22-year-old young Chinese man with vasculitis secondary to bacterial infection, which is a difficult disease to diagnose. This patient had been diagnosed with antineutrophil-cytoplasmic-antibody-negative vasculitis with pulmonary and renal involvement and was treated with glucocorticoids combined with immunosuppressive agents. However, during his follow up we found that multiple patchy shadows and cavities in both lungs and renal lesions had fluctuated, and the improvement of chest imaging was always related to antibiotic treatment. In addition, renal histology showed capillary loop necrosis and extensive crescent formation, and electron microscopy revealed scattered subepithelial hump-like deposits, which favored the diagnosis of infection over idiopathic vasculitis. Therefore, vasculitis secondary to infection was confirmed. The subsequent therapy response supported our diagnosis. This case is important; since vasculitis secondary to infection is uncommon, our case provides a model for the diagnosis of vasculitis secondary to infection.

摘要

血管炎是一组异质性的原发性疾病,可继发于多种情况。其中,由细菌感染引起的血管炎较为罕见。在此,我们展示了一名22岁中国青年男性因细菌感染继发血管炎的CT扫描图像和组织学图像,这是一种难以诊断的疾病。该患者曾被诊断为抗中性粒细胞胞浆抗体阴性的血管炎,累及肺和肾,并接受了糖皮质激素联合免疫抑制剂治疗。然而,在随访过程中,我们发现双肺多发斑片状阴影和空洞以及肾脏病变有波动,胸部影像学的改善总是与抗生素治疗有关。此外,肾脏组织学显示毛细血管袢坏死和广泛的新月体形成,电子显微镜检查发现散在的上皮下驼峰状沉积物,这更支持感染性血管炎而非特发性血管炎的诊断。因此,确诊为感染继发血管炎。后续的治疗反应支持了我们的诊断。该病例很重要;由于感染继发血管炎并不常见,我们的病例为感染继发血管炎的诊断提供了一个范例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b7f/9032307/30048cd28991/diagnostics-12-00772-g001.jpg

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