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原发性干燥综合征合并肺局限型韦格纳肉芽肿 1 例

A case of primary Sjögren's syndrome with pulmonary-limited Wegener's granulomatosis.

机构信息

Division of Rheumatology and Immunology, Department of Internal Medicine, University of Akdeniz, Antalya, Turkey.

出版信息

Rheumatol Int. 2010 Jul;30(9):1235-8. doi: 10.1007/s00296-009-1045-x. Epub 2009 Jul 4.

Abstract

A 60-year-old woman had a history of dyspnea for 5-6 weeks. The chest radiograph and computed tomography scans revealed bilateral patchy reticulonodular pattern. The patient had positive test results for antineutrophil cytoplasmic antibody against proteinase-3 (c-ANCA), antinuclear antibody and anti-Ro antibody. According to European Study Group on Classification Criteria for Sjögren's Syndrome, the patient was diagnosed as primary Sjögren's syndrome based on the presence of clinical features, positive findings on Schirmer's test and parotis scintigraphy. Lung biopsy obtained by wedge resection showed granulomatous inflammation with extensive multinuclear giant cells involving the lung parenchyma and vascular structures. There was neither upper airway nor renal involvement. Thus, the patient was simultaneously diagnosed as pulmonary-limited Wegener's granulomatosis. With this unique case, we would like to emphasize that the awareness of ANCA-associated vasculitis as a diagnostic possibility in primary Sjögren's syndrome is important during the work-up of lung lesions.

摘要

一位 60 岁女性因呼吸困难 5-6 周就诊。胸部 X 线片和 CT 扫描显示双侧斑片状网状结节模式。患者抗中性粒细胞胞浆抗体(针对蛋白酶 3 的 c-ANCA)、抗核抗体和抗 Ro 抗体检测结果阳性。根据欧洲干燥综合征分类标准研究组,该患者基于临床特征、Schirmer 试验和腮腺闪烁扫描阳性结果,被诊断为原发性干燥综合征。楔形切除获得的肺活检显示,肺实质和血管结构中存在广泛的多核巨细胞肉芽肿性炎症。无上呼吸道或肾脏受累。因此,该患者同时被诊断为肺局限型韦格纳肉芽肿。通过这个独特的病例,我们想强调在肺部病变的检查过程中,认识到抗中性粒细胞胞浆抗体相关性血管炎是原发性干燥综合征的一个诊断可能性非常重要。

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