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Immunohistochemical expression of MPO, CD163 and VEGF in inflammatory cells in acute respiratory distress syndrome: a case report
M. Maretta, S. Toth, Z. Jonecova, P. Kruzliak, P. Kubatka, S. Pingorova, J. Vesela,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu kazuistiky, časopisecké články, práce podpořená grantem
NLK
Free Medical Journals
od 2008
PubMed Central
od 2008
Europe PubMed Central
od 2008 do 2015
PubMed
25120850
Knihovny.cz E-zdroje
- MeSH
- alveolární makrofágy imunologie metabolismus MeSH
- antigeny diferenciační myelomonocytární biosyntéza MeSH
- CD antigeny biosyntéza MeSH
- dopravní nehody MeSH
- imunohistochemie MeSH
- lidé MeSH
- mimosilniční motorová vozidla MeSH
- mladý dospělý MeSH
- monocyty imunologie metabolismus MeSH
- neutrofily imunologie metabolismus MeSH
- peroxidasa biosyntéza MeSH
- pneumocyty imunologie metabolismus MeSH
- receptory buněčného povrchu biosyntéza MeSH
- syndrom dechové tísně imunologie metabolismus patologie MeSH
- vaskulární endoteliální růstový faktor A biosyntéza MeSH
- Check Tag
- lidé MeSH
- mladý dospělý MeSH
- mužské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- kazuistiky MeSH
- práce podpořená grantem MeSH
Acute respiratory distress syndrome (ARDS) is a serious medical condition occurring in patients with polytrauma, pulmonary or non-pulmonary sepsis, pneumonia and many other circumstances. It causes inflammation of the lung parenchyma leading to impaired gas exchange with a systemic release of inflammatory mediators, causing consequential lung tissue injury, hypoxemia and frequently multiple organ failure. The aim of current study was to describe expression of inflammatory markers (myeloperoxidase, CD163 and vascular endothelial growth factor) by the cells in acute phase of ARDS. The lung samples of a 20-year-old man who had suffered a serious motorbike accident were obtained for histological examination. He died on the seventh day as a consequence of respiratory failure. Our results imply that expression of CD163 was restricted to activated alveolar macrophages and monocytes. Immunopositivityof MPO was observed in neutrophil granulocytes within lung alveoli and lung blood vessels. Myeloperoxidase positivity was observed in alveolar macrophages, too. Vascular endothelial growth factor was expressed in cytoplasm of neutrophil granulocytes, monocytes, small-sized alveolar macrophages and type II pneumocytes localized mostly inside lung alveoli. On the contrary, no positivity was observed in lung endothelial cells of blood vessels.
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- $a Maretta, Milan $u Department of Histology and Embryology, Faculty of Medicine, Pavol Jozef Šafárik University Šrobárova 2, Košice, Slovak Republic.
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- $a Immunohistochemical expression of MPO, CD163 and VEGF in inflammatory cells in acute respiratory distress syndrome: a case report / $c M. Maretta, S. Toth, Z. Jonecova, P. Kruzliak, P. Kubatka, S. Pingorova, J. Vesela,
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- $a Acute respiratory distress syndrome (ARDS) is a serious medical condition occurring in patients with polytrauma, pulmonary or non-pulmonary sepsis, pneumonia and many other circumstances. It causes inflammation of the lung parenchyma leading to impaired gas exchange with a systemic release of inflammatory mediators, causing consequential lung tissue injury, hypoxemia and frequently multiple organ failure. The aim of current study was to describe expression of inflammatory markers (myeloperoxidase, CD163 and vascular endothelial growth factor) by the cells in acute phase of ARDS. The lung samples of a 20-year-old man who had suffered a serious motorbike accident were obtained for histological examination. He died on the seventh day as a consequence of respiratory failure. Our results imply that expression of CD163 was restricted to activated alveolar macrophages and monocytes. Immunopositivityof MPO was observed in neutrophil granulocytes within lung alveoli and lung blood vessels. Myeloperoxidase positivity was observed in alveolar macrophages, too. Vascular endothelial growth factor was expressed in cytoplasm of neutrophil granulocytes, monocytes, small-sized alveolar macrophages and type II pneumocytes localized mostly inside lung alveoli. On the contrary, no positivity was observed in lung endothelial cells of blood vessels.
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- $a Toth, Stefan $u Department of Histology and Embryology, Faculty of Medicine, Pavol Jozef Šafárik University Šrobárova 2, Košice, Slovak Republic.
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- $a Kruzliak, Peter $u International Clinical Research Center, St. Anne's University Hospital and Masaryk University Pekarska 53, 656 91 Brno, Czech Republic.
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- $a Kubatka, Peter $u Department of Medical Biology, Jessenius Faculty of Medicine, Comenius University Bratislava, Slovak Republic.
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- $a Pingorova, Stanislava $u Department of Traumatology, Faculty of Medicine, Pavol Jozef Šafárik University and Louis Pasteur University Hospital Rastislavova 43, Košice, Slovak Republic.
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- $a Vesela, Jarmila $u Department of Histology and Embryology, Faculty of Medicine, Pavol Jozef Šafárik University Šrobárova 2, Košice, Slovak Republic.
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