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Antemortem vs Postmortem Histopathologic and Ultrastructural Findings in Paired Transbronchial Biopsy Specimens and Lung Autopsy Samples From Three Patients With Confirmed SARS-CoV-2.
Gagiannis, Daniel; Umathum, Vincent Gottfried; Bloch, Wilhelm; Rother, Conn; Stahl, Marcel; Witte, Hanno Maximilian; Djudjaj, Sonja; Boor, Peter; Steinestel, Konrad.
  • Gagiannis D; Department of Pulmonology, Ulm, Germany.
  • Umathum VG; Institute of Pathology and Molecular Pathology, Ulm, Germany.
  • Bloch W; Department of Hematology and Oncology, Bundeswehrkrankenhaus Ulm, Ulm, Germany.
  • Rother C; Department of Molecular and Cellular Sport Medicine, German Sport University Cologne, Cologne, Germany.
  • Stahl M; Department of Pulmonology, Ulm, Germany.
  • Witte HM; Institute of Pathology and Molecular Pathology, Ulm, Germany.
  • Djudjaj S; Department of Molecular and Cellular Sport Medicine, German Sport University Cologne, Cologne, Germany.
  • Boor P; Department of Hematology and Oncology, University Hospital Schleswig-Holstein Campus Luebeck, Luebeck, Germany.
  • Steinestel K; Institute of Pathology, RWTH Aachen University Hospital, Aachen, Germany.
Am J Clin Pathol ; 157(1): 54-63, 2022 01 06.
Article in English | MEDLINE | ID: covidwho-1379433
ABSTRACT

OBJECTIVES:

Respiratory failure is the major cause of death in coronavirus disease 2019 (COVID-19). Autopsy-based reports describe diffuse alveolar damage (DAD), organizing pneumonia, and fibrotic change, but data on early pathologic changes and during progression of the disease are rare.

METHODS:

We prospectively enrolled three patients with COVID-19 and performed full clinical evaluation, including high-resolution computed tomography. We took transbronchial biopsy (TBB) specimens at different time points and autopsy tissue samples for histopathologic and ultrastructural evaluation after the patients' death.

RESULTS:

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) was confirmed by reverse transcription polymerase chain reaction and/or fluorescence in situ hybridization in all TBBs. Lung histology showed reactive pneumocytes and capillary congestion in one patient who died shortly after hospital admission with detectable virus in one of two lung autopsy samples. SARS-CoV-2 was detected in two of two autopsy samples from another patient with a fulminant course and very short latency between biopsy and autopsy, showing widespread organizing DAD. In a third patient with a prolonged course, autopsy samples showed extensive fibrosis without detectable virus.

CONCLUSIONS:

We report the course of COVID-19 in paired biopsy specimens and autopsies, illustrating vascular, organizing, and fibrotic patterns of COVID-19-induced lung injury. Our results suggest an early spread of SARS-CoV-2 from the upper airways to the lung periphery with diminishing viral load during disease.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Type of study: Experimental Studies / Prognostic study Limits: Humans Language: English Journal: Am J Clin Pathol Year: 2022 Document Type: Article Affiliation country: Ajcp

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Full text: Available Collection: International databases Database: MEDLINE Main subject: SARS-CoV-2 / COVID-19 Type of study: Experimental Studies / Prognostic study Limits: Humans Language: English Journal: Am J Clin Pathol Year: 2022 Document Type: Article Affiliation country: Ajcp