Microscopic polyangiitis-associated interstitial lung disease with acute exacerbation after SARS-CoV-2 infection: a case report and literature review.

IF 0.9 Q4 RHEUMATOLOGY
Natsuko Esa, Shogo Matsuda, Hiroko Kuwabara, Katsumasa Oe, Ayana Okazaki, Takayasu Suzuka, Yumiko Wada, Takeshi Shoda, Takuya Kotani, Tohru Takeuchi
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Abstract

Microscopic polyangiitis (MPA) is a type of systemic inflammatory small vessel vasculitis that is frequently accompanied by interstitial lung disease (ILD). Acute exacerbations (AE) of ILD are fatal complications in patients with MPA and can be triggered by various factors, including infections. We report a case of AE of MPA-ILD following severe acute respiratory syndrome Coronavirus 2 (SARS-CoV-2) infection. An 81-year-old male with MPA during remission maintenance therapy was hospitalised for Coronavirus disease 2019 pneumonia. Treatment for SARS-CoV-2 infection improved his respiratory symptoms and radiological findings, but his respiratory condition suddenly deteriorated with a high fever on hospital Day 52. Chest high-resolution computed tomography showed diffuse bilateral ground glass opacity, and we diagnosed AE of MPA-ILD. He was refractory to steroid pulse therapy and died on the second day after the onset of AE. Pathologic autopsy revealed hyaline membrane formation over the entire bilateral lobes, consistent with the exudative phase of the diffuse alveolar damage pattern. Our case suggests that persistent immune activation during the post-acute phase of SARS-CoV-2 infection may contribute to delayed AE of MPA-ILD with a diffuse alveolar damage pattern through macrophage-driven lung injury, given that ILD exacerbation occurred approximately 2 months after the onset of Coronavirus disease 2019 pneumonia.

SARS-CoV-2感染后急性加重的显微镜下多血管炎相关间质性肺疾病1例报告及文献复习
显微多血管炎(MPA)是一种全身性炎性小血管炎,常伴有间质性肺疾病(ILD)。ILD的急性加重(AE)是MPA患者的致命并发症,可由多种因素触发,包括感染。我们报告一例严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)感染后MPA-ILD的AE。1例81岁男性MPA患者在缓解维持治疗期间因2019冠状病毒病肺炎住院。对SARS-CoV-2感染的治疗改善了他的呼吸道症状和影像学检查,但在住院第52天,他的呼吸道状况突然恶化,出现高烧。胸部HRCT显示双侧弥漫性磨玻璃影,我们诊断为MPA-ILD AE。他对类固醇脉冲治疗难治性,在AE发作后第二天死亡。病理解剖显示整个双侧肺叶形成透明膜,与弥漫性肺泡损伤(DAD)的渗出相一致。我们的病例提示,SARS-CoV-2感染急性期后持续的免疫激活可能通过巨噬细胞驱动的肺损伤导致MPA-ILD具有DAD模式的延迟AE,因为ILD发作大约在COVID-19肺炎发病后两个月发生。
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CiteScore
1.40
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