髓过氧化物酶抗中性粒细胞细胞质抗体相关血管炎伴矽肺、肺泡出血和快速进行性肾小球肾炎1例报告。

IF 0.7 Q3 MEDICINE, GENERAL & INTERNAL
AME Case Reports Pub Date : 2024-10-24 eCollection Date: 2025-01-01 DOI:10.21037/acr-24-112
Keiichi Mizuhashi
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引用次数: 0

摘要

背景:一些职业病如矽肺的潜在病理生理机制与自身抗体有关。一种自身抗体,抗中性粒细胞胞浆抗体(ANCA),最近有报道,已知在血管炎等疾病中升高;因此,这种疾病目前被称为anca相关性血管炎。已知矽肺患者发生anca相关血管炎的风险是无任何职业病患者的25倍。在本报告中,作者描述了一例男性矽肺后发展为anca相关血管炎,导致严重的肺泡出血和肾功能障碍。病例描述:一名日本男子,50多岁,从事隧道施工33年,主诉为咳嗽带痰。根据胸部图像和他的职业史,诊断为矽肺病。2008年11月检出尿隐血;因此,测定骨髓过氧化物酶抗中性粒细胞胞浆抗体(MPO-ANCA)水平(15.9 U/mL)。2009年9月,他出现全身疲劳、发热、盗汗、痰血和呼吸困难。胸部图像显示新的阴影,MPO-ANCA水平升高至690 U/mL。支气管肺泡灌洗液带血,证实肺泡出血。血痰自然溶解;然而,随后观察到血清肌酐水平短期升高。肾活检证实坏死性新月形肾小球肾炎。因此,他被诊断为mpo - anca相关性血管炎伴矽肺、肺泡出血和快速进行性肾小球肾炎。经甲泼尼龙琥珀酸钠和环磷酰胺脉冲联合治疗后缓解。结论:对于伴有痰血或其他症状的矽肺患者,除考虑结核、肺癌外,还应考虑anca相关性血管炎。也有必要密切关注可能发生的快速进展的肾小球肾炎,因为它有时是致命的。此外,在对快速进展性肾小球肾炎患者进行检查时,必须注意患者以前是否接触过二氧化硅粉尘,无论是否职业性接触。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Myeloperoxidase anti-neutrophil cytoplasmic antibody-associated vasculitis with silicosis, alveolar hemorrhage, and rapidly progressive glomerulonephritis: a case report.

Background: The underlying pathophysiology of some occupational diseases such as silicosis involves autoantibodies. An autoantibody, antineutrophil cytoplasmic antibody (ANCA), has been recently reported and is known to be elevated in diseases such as vasculitis; therefore, the disease is currently known as ANCA-associated vasculitis. The risk of ANCA-associated vasculitis is known to be 25 times higher in patients with silicosis than in those without any occupational disease. In this report, the author describes the case of a man who developed ANCA-associated vasculitis after silicosis, leading to severe alveolar hemorrhage and renal dysfunction.

Case description: A Japanese man in his 50s who was engaged in tunnel construction for 33 years presented with the chief complaint of cough with sputum. Based on chest images and his occupational history, a diagnosis of silicosis was made. In November 2008, urinary occult blood was detected; therefore, myeloperoxidase anti-neutrophil cytoplasmic antibody (MPO-ANCA) levels were measured (15.9 U/mL). In September 2009, he experienced systemic fatigue, fever, night sweats, bloody sputum, and difficulty breathing. Chest images showed new shadows, and MPO-ANCA levels had increased to 690 U/mL. His bronchoalveolar lavage fluid was bloody, confirming alveolar hemorrhage. The bloody sputum resolved spontaneously; however, a subsequent short-term increase in serum creatinine levels was observed. Renal biopsy confirmed necrotizing crescentic glomerulonephritis. Therefore, he was diagnosed with MPO-ANCA-associated vasculitis with silicosis, alveolar hemorrhage, and rapidly progressive glomerulonephritis. Treatment with combination therapy of pulse methylprednisolone sodium succinate and cyclophosphamide led to remission.

Conclusions: For patients with silicosis, accompanied by bloody sputum or other symptoms, ANCA-associated vasculitis, besides tuberculosis and lung cancer, should be considered. It is also necessary to pay close attention to the possible onset of rapidly progressive glomerulonephritis because it is sometimes fatal. In addition, when examining a patient with rapidly progressive glomerulonephritis, attention must be paid to whether the patient has had previous exposure to silica dust, regardless of whether or not the exposure was occupational.

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