Pulmonary pathological features in coronavirus associated severe acute respiratory syndrome (SARS).
Identifieur interne : 002F34 ( PubMed/Curation ); précédent : 002F33; suivant : 002F35Pulmonary pathological features in coronavirus associated severe acute respiratory syndrome (SARS).
Auteurs : G M-K Tse [République populaire de Chine] ; K-F To ; P K-S Chan ; A W I. Lo ; K-C Ng ; A. Wu ; N. Lee ; H-C Wong ; S-M Mak ; K-F Chan ; D S C. Hui ; J J-Y Sung ; H-K NgSource :
- Journal of clinical pathology [ 0021-9746 ] ; 2004.
Descripteurs français
- KwdFr :
- Adulte, Adulte d'âge moyen, Alvéoles pulmonaires (anatomopathologie), Cellules cultivées, Coronavirus (isolement et purification), Division cellulaire, Femelle, Humains, Immunohistochimie (), Microscopie électronique, Mâle, Noyau de la cellule (anatomopathologie), Poumon (anatomopathologie), Poumon (virologie), Sujet âgé, Sujet âgé de 80 ans ou plus, Syndrome respiratoire aigu sévère (anatomopathologie), Syndrome respiratoire aigu sévère (virologie).
- MESH :
- anatomopathologie : Alvéoles pulmonaires, Noyau de la cellule, Poumon, Syndrome respiratoire aigu sévère.
- isolement et purification : Coronavirus.
- virologie : Poumon, Syndrome respiratoire aigu sévère.
- Adulte, Adulte d'âge moyen, Cellules cultivées, Division cellulaire, Femelle, Humains, Immunohistochimie, Microscopie électronique, Mâle, Sujet âgé, Sujet âgé de 80 ans ou plus.
English descriptors
- KwdEn :
- Adult, Aged, Aged, 80 and over, Cell Division, Cell Nucleus (pathology), Cells, Cultured, Coronavirus (isolation & purification), Female, Humans, Immunohistochemistry (methods), Lung (pathology), Lung (virology), Male, Microscopy, Electron, Middle Aged, Pulmonary Alveoli (pathology), Severe Acute Respiratory Syndrome (pathology), Severe Acute Respiratory Syndrome (virology).
- MESH :
- isolation & purification : Coronavirus.
- methods : Immunohistochemistry.
- pathology : Cell Nucleus, Lung, Pulmonary Alveoli, Severe Acute Respiratory Syndrome.
- virology : Lung, Severe Acute Respiratory Syndrome.
- Adult, Aged, Aged, 80 and over, Cell Division, Cells, Cultured, Female, Humans, Male, Microscopy, Electron, Middle Aged.
Abstract
Severe acute respiratory syndrome (SARS) became a worldwide outbreak with a mortality of 9.2%. This new human emergent infectious disease is dominated by severe lower respiratory illness and is aetiologically linked to a new coronavirus (SARS-CoV).
DOI: 10.1136/jcp.2003.013276
PubMed: 14990596
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pubmed:14990596Le document en format XML
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<term>Severe Acute Respiratory Syndrome</term>
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<term>Syndrome respiratoire aigu sévère</term>
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<front><div type="abstract" xml:lang="en">Severe acute respiratory syndrome (SARS) became a worldwide outbreak with a mortality of 9.2%. This new human emergent infectious disease is dominated by severe lower respiratory illness and is aetiologically linked to a new coronavirus (SARS-CoV).</div>
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<DateCompleted><Year>2004</Year>
<Month>03</Month>
<Day>31</Day>
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<DateRevised><Year>2019</Year>
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<Title>Journal of clinical pathology</Title>
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<ArticleTitle>Pulmonary pathological features in coronavirus associated severe acute respiratory syndrome (SARS).</ArticleTitle>
<Pagination><MedlinePgn>260-5</MedlinePgn>
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<Abstract><AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Severe acute respiratory syndrome (SARS) became a worldwide outbreak with a mortality of 9.2%. This new human emergent infectious disease is dominated by severe lower respiratory illness and is aetiologically linked to a new coronavirus (SARS-CoV).</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">Pulmonary pathology and clinical correlates were investigated in seven patients who died of SARS in whom there was a strong epidemiological link. Investigations include a review of clinical features, morphological assessment, histochemical and immunohistochemical stainings, ultrastructural study, and virological investigations in postmortem tissue.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">Positive viral culture for coronavirus was detected in most premortem nasopharyngeal aspirate specimens (five of six) and postmortem lung tissues (two of seven). Viral particles, consistent with coronavirus, could be detected in lung pneumocytes in most of the patients. These features suggested that pneumocytes are probably the primary target of infection. The pathological features were dominated by diffuse alveolar damage, with the presence of multinucleated pneumocytes. Fibrogranulation tissue proliferation in small airways and airspaces (bronchiolitis obliterans organising pneumonia-like lesions) in subpleural locations was also seen in some patients.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">Viable SARS-CoV could be isolated from postmortem tissues. Postmortem examination allows tissue to be sampled for virological investigations and ultrastructural examination, and when coupled with the appropriate lung morphological changes, is valuable to confirm the diagnosis of SARS-CoV, particularly in clinically unapparent or suspicious but unconfirmed cases.</AbstractText>
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