Department of Pathology, University of Michigan, Ann Arbor, MI, USA.
Histopathology. 2020 Oct;77(4):570-578. doi: 10.1111/his.14180. Epub 2020 Sep 12.
AIMS: Diffuse alveolar damage (DAD) is a ubiquitous finding in inpatient coronavirus disease 2019 (COVID-19)-related deaths, but recent reports have also described additional atypical findings, including vascular changes. An aim of this study was to assess lung autopsy findings in COVID-19 inpatients, and in untreated severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-positive individuals who died in the community, in order to understand the relative impact of medical intervention on lung histology. Additionally, we aimed to investigate whether COVID-19 represents a unique histological variant of DAD by comparing the pathological findings with those of uninfected control patients. METHODS AND RESULTS: Lung sections from autopsy cases were reviewed by three pulmonary pathologists, including two who were blinded to patient cohort. The cohorts included four COVID-19 inpatients, four cases with postmortem SARS-CoV-2 diagnoses who died in the community, and eight SARS-CoV-2-negative control cases. DAD was present in all but one SARS-CoV-2-positive patient, who was asymptomatic and died in the community. Although SARS-CoV-2-positive patients were noted to have more focal perivascular inflammation/endothelialitis than control patients, there were no significant differences in the presence of hyaline membranes, fibrin thrombi, airspace organisation, and 'acute fibrinous and organising pneumonia'-like intra-alveolar fibrin deposition between the cohorts. Fibrinoid vessel wall necrosis, haemorrhage and capillaritis were not features of COVID-19-related DAD. CONCLUSIONS: DAD is the primary histological manifestation of severe lung disease in COVID-19 patients who die both in hospital and in the community, suggesting no contribution of hyperoxaemic mechanical ventilation to the histological changes. There are no distinctive morphological features with which to confidently differentiate COVID-19-related DAD from DAD due to other causes.
目的:弥漫性肺泡损伤(DAD)是 2019 年冠状病毒病(COVID-19)相关住院患者死亡的普遍发现,但最近的报告也描述了其他非典型发现,包括血管变化。本研究的目的是评估 COVID-19 住院患者和未经治疗的社区中死于严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)阳性个体的肺尸检结果,以了解医疗干预对肺组织学的相对影响。此外,我们旨在通过将病理发现与未感染对照患者的发现进行比较,来研究 COVID-19 是否代表 DAD 的独特组织学变体。
方法和结果:由三位肺病理学家对尸检病例的肺切片进行了评估,其中两位病理学家对患者队列不知情。队列包括 4 名 COVID-19 住院患者、4 名死于社区的死后 SARS-CoV-2 诊断患者和 8 名 SARS-CoV-2 阴性对照患者。除了一名无症状且死于社区的 SARS-CoV-2 阳性患者外,所有患者均存在 DAD。尽管 SARS-CoV-2 阳性患者的血管周围炎症/内皮炎比对照患者更具局灶性,但两组之间透明膜、纤维蛋白血栓、气腔组织和“急性纤维蛋白性和机化性肺炎”样肺泡内纤维蛋白沉积的存在没有显著差异。纤维蛋白样血管壁坏死、出血和毛细血管炎不是 COVID-19 相关 DAD 的特征。
结论:DAD 是 COVID-19 患者死亡的严重肺部疾病的主要组织学表现,无论是在医院还是在社区死亡,这表明高氧机械通气对组织学变化没有贡献。没有独特的形态学特征可以自信地区分 COVID-19 相关 DAD 与其他原因引起的 DAD。
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