显微多血管炎合并矽肺1例。

Masaki Nakanishi, Koji Date, Yasunori Koyama, Mikio Ueda, Taichiro Arimoto, Yoshinobu Iwasaki
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引用次数: 0

摘要

一名76岁男性因肺结节增大而入院,同时在另一家医院因矽肺病接受观察。经支气管镜活检证实为矽肺结节。然而,大约一个月后,他因左侧自发性气胸再次住院。通过持续胸腔引流,气胸立即得到改善,但他在第9天出现发烧,尽管我们给予抗生素治疗,双肺的磨玻璃混浊也加剧了。MPO-ANCA水平明显升高,第29天右大腿可见多发3-10mm大小紫癜。皮肤活检显示真皮下部中等血管周围有组织细胞和淋巴细胞浸润。我们诊断为显微镜下的多血管炎,然后用类固醇和免疫抑制治疗。发热和影像学表现从类固醇给药后的第一天起显著改善。病人因呼吸情况好转,于第92天出院。我们报告一例显微多血管炎合并矽肺,经类固醇及免疫抑制治疗后明显改善。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[A case of microscopic polyangiitis with silicosis].

A 76-year-old man was admitted to our hospital because of increasing size of lung nodules, while he was under observation for silicosis at another hospital. As the result of bronchoscopic biopsy, it was confirmed that they were silicotic nodules. However, he was hospitalized again about one month later due to left spontaneous pneumothorax. The pneumothorax improved immediately by persistent drainage of the thoracic cavity, but he developed a fever on day 9, and ground-glass opacities in both lungs also became exacerbated in spite of our administration of antibiotics. In addition, the level of MPO-ANCA increased markedly and multiple 3-10mm sized purpurae was seen on the right thigh on day 29. Skin biopsy specimens revealed infiltration of histiocytes and lymphocytes around medium-sized vessels in lower dermis. We diagnosed microscopic polyangiitis, then treated with steroid and immunosuppressive therapy. Fever and radiological findings improved significantly from the day after initiation of steroid administration. The patient was discharged on day 92 because of the improvement of his respiratory condition. We report a case of microscopic polyangiitis with silicosis, which markedly improved by steroid and immunosuppressive therapy.

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