Department of Internal Medicine, Connective Tissue Diseases and Geriatrics, Medical University of Gdansk, Gdansk, Poland.
PLoS One. 2019 Sep 10;14(9):e0222189. doi: 10.1371/journal.pone.0222189. eCollection 2019.
Granulomatosis with polyangiitis (GPA) and microscopic polyangiitis (MPA) are forms of antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV). AAV most commonly affects the upper and lower respiratory tract as well as the kidneys. The first symptoms are often nonspecific, requiring careful differential diagnosis with infections and malignancies.
We analyzed the clinical and radiological data of 38 patients (20 females and 18 males) diagnosed with ANCA-associated vasculitis. Lung involvement was observed in 29 cases. Lung ultrasound (LUS) was performed on 21 patients from the study group and compared to chest CT. For 7 patients the examination was conducted repeatedly.
In total, 35 LUS and CT examinations were performed, revealing the following lesions: nodules, infiltrates with and without features of disintegration, caves (n = 17), diffuse alveolar hemorrhage (n = 3), and features of interstitial lung disease (ILD) with pulmonary fibrosis (PF) (n = 11). In 2 cases LUS and CT were negative. In 4 cases LUS was negative, despite a positive CT result.
Both in CT and LUS, images of pulmonary lesions were consistent though highly variable. Therefore, further studies are required for a larger group of patients.
肉芽肿性多血管炎(GPA)和显微镜下多血管炎(MPA)是抗中性粒细胞胞质抗体(ANCA)相关性血管炎(AAV)的两种形式。AAV 最常影响上呼吸道和下呼吸道以及肾脏。最初的症状通常是非特异性的,需要与感染和恶性肿瘤进行仔细的鉴别诊断。
我们分析了 38 名(20 名女性和 18 名男性)诊断为 ANCA 相关性血管炎的患者的临床和影像学数据。29 例患者存在肺部受累。对 21 名研究组患者进行了肺部超声(LUS)检查,并与胸部 CT 进行了比较。对 7 名患者进行了重复检查。
共进行了 35 次 LUS 和 CT 检查,发现了以下病变:结节、伴有或不伴有崩解特征的浸润、空洞(n=17)、弥漫性肺泡出血(n=3)、伴有肺纤维化(PF)的间质性肺病(ILD)特征(n=11)。2 例 LUS 和 CT 均为阴性。4 例 LUS 为阴性,尽管 CT 结果为阳性。
在 CT 和 LUS 中,肺部病变的图像虽然高度可变,但一致。因此,需要对更大的患者群体进行进一步的研究。