[Segmental Bronchoalveolar Lavage Provided a Favorable Clinical Course in a Case of Autoimmune Pulmonary Alveolar Proteinosis].

Q3 Medicine
T. Manabe, Rintaro Oyama, Yudai Yamaguchi, T. Hanagiri
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引用次数: 0

Abstract

A 49-year-old man was diagnosed with autoimmune pulmonary alveolar proteinosis. Chest computed tomography (CT) showed typical CT findings of pulmonary alveolar proteinosis: thickening of septa with ground-glass opacities in both lung fields. The diagnosis of autoimmune pulmonary alveolar proteinosis (PAP) was based on findings of bronchoalveolar lavage (BAL) fluid with milky appearance and elevated serum titer of anti-granulocyte-macrophage colony-stimulating factor antibody. We decided to perform segmental BAL via bronchoscopy. The surgery was performed under a general anesthesia since the patient had severe hypoxemia and strong cough reflex. Following 3 repeated courses of therapy, his respiratory condition and the ground-glass opacity in both lung fields improved remarkably, with no recurrence in 3 years. There are only a few published case reports in the world of the usefulness of segmental BAL under general anesthesia for PAP. We consider that segmental BAL is a useful therapeutic method for PAP in cases with severe hypoxemia, such as the present patient.
【段性支气管肺泡灌洗治疗自身免疫性肺泡蛋白沉积症1例】。
一名49岁男子被诊断为自身免疫性肺泡蛋白沉积症。胸部计算机断层扫描(CT)显示肺泡蛋白沉积症的典型CT表现:两肺野纵隔增厚并磨玻璃样阴影。自身免疫性肺泡蛋白沉积症(PAP)的诊断是基于支气管肺泡灌洗液的乳白色外观和抗粒细胞-巨噬细胞集落刺激因子抗体的血清滴度升高。我们决定通过支气管镜进行节段性支气管镜检查。手术是在全身麻醉下进行的,因为患者有严重的低氧血症和强烈的咳嗽反射。经过3个疗程的反复治疗,他的呼吸系统状况和两个肺野的磨玻璃样混浊明显改善,3年内没有复发。世界上只有少数已发表的病例报告表明,在全身麻醉下分段BAL对PAP有用。我们认为节段性BAL是治疗严重低氧血症患者(如本患者)PAP的有效方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of UOEH
Journal of UOEH Medicine-Medicine (all)
CiteScore
1.30
自引率
0.00%
发文量
35
期刊介绍: Published quarterly: 1 annual volume consisted of 4 numbers. Issued on the 1st of March, June, September and December, respectively.
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