Abstract

BackgroundSevere COVID-19 has a high mortality rate. Comprehensive pathological descriptions of COVID-19 are scarce and limited in scope. We aimed to describe the histopathological findings and viral tropism in patients who died of severe COVID-19.MethodsIn this case series, patients were considered eligible if they were older than 18 years, with premortem diagnosis of severe acute respiratory syndrome coronavirus 2 infection and COVID-19 listed clinically as the direct cause of death. Between March 1 and April 30, 2020, full post-mortem examinations were done on nine patients with confirmed COVID-19, including sampling of all major organs. A limited autopsy was done on one additional patient. Histochemical and immunohistochemical analyses were done, and histopathological findings were reported by subspecialist pathologists. Viral quantitative RT-PCR analysis was done on tissue samples from a subset of patients.FindingsThe median age at death of our cohort of ten patients was 73 years (IQR 52–79). Thrombotic features were observed in at least one major organ in all full autopsies, predominantly in the lung (eight [89%] of nine patients), heart (five [56%]), and kidney (four [44%]). Diffuse alveolar damage was the most consistent lung finding (all ten patients); however, organisation was noted in patients with a longer clinical course. We documented lymphocyte depletion (particularly CD8-positive T cells) in haematological organs and haemophagocytosis. Evidence of acute tubular injury was noted in all nine patients examined. Major unexpected findings were acute pancreatitis (two [22%] of nine patients), adrenal micro-infarction (three [33%]), pericarditis (two [22%]), disseminated mucormycosis (one [10%] of ten patients), aortic dissection (one [11%] of nine patients), and marantic endocarditis (one [11%]). Viral genomes were detected outside of the respiratory tract in four of five patients. The presence of subgenomic viral RNA transcripts provided evidence of active viral replication outside the respiratory tract in three of five patients.InterpretationOur series supports clinical data showing that the four dominant interrelated pathological processes in severe COVID-19 are diffuse alveolar damage, thrombosis, haemophagocytosis, and immune cell depletion. Additionally, we report here several novel autopsy findings including pancreatitis, pericarditis, adrenal micro-infarction, secondary disseminated mucormycosis, and brain microglial activation, which require additional investigation to understand their role in COVID-19.FundingImperial Biomedical Research Centre, Wellcome Trust, Biotechnology and Biological Sciences Research Council.

Highlights

  • In the UK, the death toll from severe COVID-19 is among the highest worldwide.[1]

  • Severe COVID-19 is characterised by respiratory failure, with so-called cytokine storm occurring in some patient subsets.[2]

  • COVID-19 is caused by infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2).[4,5]

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Summary

Introduction

In the UK, the death toll from severe COVID-19 is among the highest worldwide.[1]. Severe COVID-19 is characterised by respiratory failure, with so-called cytokine storm occurring in some patient subsets.[2]. Autopsy-based histopathological analysis is crucial in this respect. COVID-19 is caused by infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2).[4,5] SARS-CoV-2 and its predecessor SARS-CoV (causing severe acute respiratory syndrome [SARS]) are similar on a molecular and clinical level, COVID-19 has a lower death rate (4% for COVID-19 vs 15% for SARS) and a substantially higher death toll (700 539 deaths worldwide from COVID-19 as of Aug 5, 2020 vs 774 from SARS) than SARS due to a higher basic reproduction number.[1] The post-mortem findings in patients with SARS-CoV infection included diffuse alveolar damage (DAD), splenic and nodal lymphocyte depletion, haemophagocytosis, renal acute tubular injury, cerebral oedema, micro-thrombosis, and adrenalitis with necrosis, with intracellular SARS-CoV detected in the lungs, kidney, brain, and haematological organs.[6] Various autopsy series on COVID-19 have begun to emerge in the literature.[7,8,9,10,11,12,13,14,15] Here, we document the major pathological

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