Autopsy Findings in 32 Patients with COVID-19: A Single-Institution Experience.


Journal

Pathobiology : journal of immunopathology, molecular and cellular biology
ISSN: 1423-0291
Titre abrégé: Pathobiology
Pays: Switzerland
ID NLM: 9007504

Informations de publication

Date de publication:
2021
Historique:
received: 03 07 2020
accepted: 24 08 2020
pubmed: 18 9 2020
medline: 24 2 2021
entrez: 17 9 2020
Statut: ppublish

Résumé

A novel coronavirus, SARS-CoV-2, was identified in Wuhan, China in late 2019. This virus rapidly spread around the world causing disease ranging from minimal symptoms to severe pneumonia, which was termed coronavirus disease (i.e., COVID). Postmortem examination is a valuable tool for studying the pathobiology of this new infection. We report the clinicopathologic findings from 32 autopsy studies conducted on patients who died of COVID-19 including routine gross and microscopic examination with applicable special and immunohistochemical staining techniques. SARS-CoV-2 infection was confirmed by nasopharyngeal RT-PCR in 31 cases (97%) and by immunohistochemical staining for SARS-CoV-2 spike-protein in the lung in the remaining 1 case (3%). The ethnically diverse cohort consisted of 22 males and 10 females with a mean age of 68 years (range: 30-100). Patients most commonly presented with cough (17 [55%]), shortness of breath (26 [81%]), and a low-grade fever (17 [55%]). Thirty-one (97%) of the patients had at least 1 comorbidity (mean = 4). Twenty-eight patients (88%) had widespread thromboembolic disease, as well as diffuse alveolar damage (30 [94%]), diabetic nephropathy (17 [57%]) and acute tubular injury. Patterns of liver injury were heterogeneous, featuring 10 (36%) with frequent large basophilic structures in sinusoidal endothelium, and increased immunoblast-like cells in lymph nodes. This series of autopsies from patients with COVID-19 confirms the observation that the majority of severely affected patients have significant pulmonary pathology. However, many patients also have widespread microscopic thromboses, as well as characteristic findings in the liver and lymph nodes.

Sections du résumé

BACKGROUND BACKGROUND
A novel coronavirus, SARS-CoV-2, was identified in Wuhan, China in late 2019. This virus rapidly spread around the world causing disease ranging from minimal symptoms to severe pneumonia, which was termed coronavirus disease (i.e., COVID). Postmortem examination is a valuable tool for studying the pathobiology of this new infection.
METHODS METHODS
We report the clinicopathologic findings from 32 autopsy studies conducted on patients who died of COVID-19 including routine gross and microscopic examination with applicable special and immunohistochemical staining techniques.
RESULTS RESULTS
SARS-CoV-2 infection was confirmed by nasopharyngeal RT-PCR in 31 cases (97%) and by immunohistochemical staining for SARS-CoV-2 spike-protein in the lung in the remaining 1 case (3%). The ethnically diverse cohort consisted of 22 males and 10 females with a mean age of 68 years (range: 30-100). Patients most commonly presented with cough (17 [55%]), shortness of breath (26 [81%]), and a low-grade fever (17 [55%]). Thirty-one (97%) of the patients had at least 1 comorbidity (mean = 4). Twenty-eight patients (88%) had widespread thromboembolic disease, as well as diffuse alveolar damage (30 [94%]), diabetic nephropathy (17 [57%]) and acute tubular injury. Patterns of liver injury were heterogeneous, featuring 10 (36%) with frequent large basophilic structures in sinusoidal endothelium, and increased immunoblast-like cells in lymph nodes.
CONCLUSION CONCLUSIONS
This series of autopsies from patients with COVID-19 confirms the observation that the majority of severely affected patients have significant pulmonary pathology. However, many patients also have widespread microscopic thromboses, as well as characteristic findings in the liver and lymph nodes.

Identifiants

pubmed: 32942274
pii: 000511325
doi: 10.1159/000511325
pmc: PMC7573917
doi:

Substances chimiques

Spike Glycoprotein, Coronavirus 0
spike protein, SARS-CoV-2 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

56-68

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2020 The Author(s) Published by S. Karger AG, Basel.

Auteurs

Sarah S Elsoukkary (SS)

Department of Pathology and Laboratory Medicine, NewYork-Presbyterian Hospital, New York, New York, USA.

Maria Mostyka (M)

Department of Pathology and Laboratory Medicine, NewYork-Presbyterian Hospital, New York, New York, USA.

Alicia Dillard (A)

Department of Pathology and Laboratory Medicine, NewYork-Presbyterian Hospital, New York, New York, USA.

Diana R Berman (DR)

Department of Pathology and Laboratory Medicine, NewYork-Presbyterian Hospital, New York, New York, USA.

Lucy X Ma (LX)

Department of Pathology and Laboratory Medicine, NewYork-Presbyterian Hospital, New York, New York, USA.

Amy Chadburn (A)

Weill Cornell Medicine, New York, New York, USA.

Rhonda K Yantiss (RK)

Weill Cornell Medicine, New York, New York, USA.

Jose Jessurun (J)

Weill Cornell Medicine, New York, New York, USA.

Surya V Seshan (SV)

Weill Cornell Medicine, New York, New York, USA.

Alain C Borczuk (AC)

Weill Cornell Medicine, New York, New York, USA.

Steven P Salvatore (SP)

Weill Cornell Medicine, New York, New York, USA, sts9057@med.cornell.edu.

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Classifications MeSH