Pulmonary fibrosis predating microscopic polyangiitis by seven years

Angeliki M. Tsimogianni, Magda Stratiki, Grigoris Stratakos, Spyros Zakynthinos, Paraskeyi Katsaounou
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引用次数: 1

Abstract

A 63-year-old man, ex-smoker with renal failure of recent onset was admitted at the respiratory department with massive haemoptysis. Previous X-rays and CT scans showed pulmonary fibrosis of seven-year duration. Subsequently, he developed high fever, large haemoptysis, new infiltrates and respiratory failure despite broad-spectrum antibiotic treatment. Antineutrophilic antibodies of the perinuclear type with specificity against myeloperoxidase were detected and microscopic polyangiitis was diagnosed. Immunosuppressive treatment with methylprednisolone pulses and cyclophosphamide was started with initially favorable response, but later the patient developed a hospital-acquired pneumonia which was treated successfully with meropenem. As pulmonary haemorrhage recurred, he was transferred to intensive care for plasmapheresis which was considered the last treatment option. Unfortunately he died from septic shock.

Conclusion

Asymptomatic pulmonary fibrosis can predate microscopic polyangiitis by several years and is associated with unfavorable prognosis of the vasculitis. Appreciation of this finding would lead to faster diagnosis and better management of these patients.

肺纤维化比显微镜下多血管炎早7年
63岁男性,前吸烟者,近期肾衰竭,因大量咯血住进呼吸科。之前的x光和CT扫描显示肺纤维化持续了7年。随后,尽管广谱抗生素治疗,他仍出现高热、大咯血、新的浸润和呼吸衰竭。检测到特异性抗髓过氧化物酶的核周型抗中性粒细胞抗体,镜下诊断为多血管炎。甲泼尼龙脉冲和环磷酰胺的免疫抑制治疗开始时效果良好,但后来患者发展为医院获得性肺炎,用美罗培南治疗成功。由于肺出血复发,他被转移到重症监护室进行血浆置换,这是最后的治疗选择。不幸的是,他死于感染性休克。结论无症状肺纤维化可早于显微镜下多血管炎发生数年,且与血管炎预后不良有关。对这一发现的赞赏将导致更快的诊断和更好的管理这些患者。
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