Hypopharyngeal Ulcers in COVID-19: Histopathological and Virological Analyses - A Case Report.
Aged
Antigens, CD
/ metabolism
Antigens, Differentiation, Myelomonocytic
/ metabolism
Autopsy
Blood Platelets
/ metabolism
COVID-19
/ complications
Gastrointestinal Tract
/ pathology
Herpesvirus 1, Human
/ genetics
Humans
Hypopharynx
/ pathology
Immunohistochemistry
Inflammation
/ immunology
Lymphocytes
/ metabolism
Monocytes
/ metabolism
Mucous Membrane
/ pathology
Muscle, Skeletal
/ pathology
Necrosis
/ pathology
SARS-CoV-2
/ genetics
Spike Glycoprotein, Coronavirus
/ metabolism
Thrombosis
/ pathology
Ulcer
/ pathology
COVID-19
HSV
gastrointestinal tract
histopathology
inflammation
molecular analysis
mucosal injury
Journal
Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960
Informations de publication
Date de publication:
2021
2021
Historique:
received:
06
03
2021
accepted:
21
06
2021
entrez:
22
7
2021
pubmed:
23
7
2021
medline:
10
8
2021
Statut:
epublish
Résumé
In coronavirus disease 2019 (COVID-19), ulcerative lesions have been episodically reported in various segments of the gastrointestinal (GI) tract, including the oral cavity, oropharynx, esophagus, stomach and bowel. In this report, we describe an autopsy case of a COVID-19 patient who showed two undiagnosed ulcers at the level of the anterior and posterior walls of the hypopharynx. Molecular testing of viruses involved in pharyngeal ulcers demonstrated the presence of severe acute respiratory syndrome - coronavirus type 2 (SARS-CoV-2) RNA, together with herpes simplex virus 1 DNA. Histopathologic analysis demonstrated full-thickness lympho-monocytic infiltration (mainly composed of CD68-positive cells), with hemorrhagic foci and necrosis of both the mucosal layer and deep skeletal muscle fibers. Fibrin and platelet microthrombi were also found. Cytological signs of HSV-1 induced damage were not found. Cells expressing SARS-CoV-2 spike subunit 1 were immunohistochemically identified in the inflammatory infiltrations. Immunohistochemistry for HSV1 showed general negativity for inflammatory infiltration, although in the presence of some positive cells. Thus, histopathological, immunohistochemical and molecular findings supported a direct role by SARS-CoV-2 in producing local ulcerative damage, although a possible contributory role by HSV-1 reactivation cannot be excluded. From a clinical perspective, this autopsy report of two undiagnosed lesions put the question if ulcers along the GI tract could be more common (but frequently neglected) in COVID-19 patients.
Identifiants
pubmed: 34290701
doi: 10.3389/fimmu.2021.676828
pmc: PMC8287416
doi:
Substances chimiques
Antigens, CD
0
Antigens, Differentiation, Myelomonocytic
0
CD68 antigen, human
0
Spike Glycoprotein, Coronavirus
0
spike protein, SARS-CoV-2
0
Types de publication
Case Reports
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
676828Informations de copyright
Copyright © 2021 Porzionato, Stocco, Emmi, Contran, Macchi, Riccetti, Sinigaglia, Barzon and De Caro.
Déclaration de conflit d'intérêts
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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