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10.1007/s00428-020-02881-x

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suck abstract from ncbi


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pmid32607684      Virchows+Arch 2020 ; 477 (3): 349-357
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  • The evolution of pulmonary pathology in fatal COVID-19 disease: an autopsy study with clinical correlation #MMPMID32607684
  • Bosmuller H; Traxler S; Bitzer M; Haberle H; Raiser W; Nann D; Frauenfeld L; Vogelsberg A; Klingel K; Fend F
  • Virchows Arch 2020[Sep]; 477 (3): 349-357 PMID32607684show ga
  • The pandemia of coronavirus disease 2019 (COVID-19) has caused more than 355,000 confirmed deaths worldwide. However, publications on postmortem findings are scarce. We present the pulmonary findings in four cases of fatal COVID-19 with a spectrum of lung pathology reflecting disease course and duration, invasive therapies, and laboratory features. Early disease is characterized by neutrophilic, exudative capillaritis with microthrombosis and high levels of IL-1beta and IL-6. Later stages are associated with diffuse alveolar damage and ongoing intravascular thrombosis in small to medium-sized pulmonary vessels, occasionally with areas of infarction equivalents, accompanied by laboratory features of disseminated intravascular coagulation. In late stages, organizing pneumonia with extensive intra-alveolar proliferation of fibroblasts and marked metaplasia of alveolar epithelium can be observed. Viral RNA is encountered in the lung, with virus particles in endothelial cells and pneumocytes. In many patients, multi-organ failure with severe liver damage sets in finally, possibly as consequence of an early-onset pro-inflammatory cytokine storm and/or thrombotic microangiopathy.
  • |Aged[MESH]
  • |Autopsy[MESH]
  • |Betacoronavirus[MESH]
  • |COVID-19[MESH]
  • |Coronavirus Infections/*pathology[MESH]
  • |Female[MESH]
  • |Humans[MESH]
  • |Lung Diseases/*pathology/*virology[MESH]
  • |Male[MESH]
  • |Middle Aged[MESH]
  • |Pandemics[MESH]
  • |Pneumonia, Viral/*pathology[MESH]
  • |SARS-CoV-2[MESH]


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