[Isolation of Geosmithia argillacea in a cystic fibrosis patient].
Identifieur interne : 000156 ( PubMed/Corpus ); précédent : 000155; suivant : 000157[Isolation of Geosmithia argillacea in a cystic fibrosis patient].
Auteurs : F. Labbé ; S. Babchia ; F. Evreux ; P. ChenalSource :
- Journal de mycologie medicale [ 1773-0449 ] ; 2013.
English descriptors
- KwdEn :
- MESH :
- complications : Cystic Fibrosis, Lung Diseases, Fungal.
- isolation & purification : Eurotiales.
- microbiology : Cystic Fibrosis, Lung Diseases, Fungal, Sputum.
- Child, Humans, Male.
Abstract
We report the case of an 11-year-old child with cystic fibrosis where Geosmithia argillacea has been isolated from sputum. This is a filamentous fungus (mold) recently described as emergent infectious agent in cystic fibrosis patients. In our case, the presence of G. argillacea was not associated with clinical disorder. However, recent evidence shows that it can be responsible for very serious invasive infection, especially in chronic granulomatous disease and may be, after lung transplantation.
DOI: 10.1016/j.mycmed.2013.05.003
PubMed: 23856446
Links to Exploration step
pubmed:23856446Le document en format XML
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<affiliation><nlm:affiliation>Laboratoire de microbiologie, hôpital J. Monod, groupe hospitalier du Havre, Le Havre cedex, France. franck.labbe@ch-havre.fr</nlm:affiliation>
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<author><name sortKey="Babchia, S" sort="Babchia, S" uniqKey="Babchia S" first="S" last="Babchia">S. Babchia</name>
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<author><name sortKey="Evreux, F" sort="Evreux, F" uniqKey="Evreux F" first="F" last="Evreux">F. Evreux</name>
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<author><name sortKey="Chenal, P" sort="Chenal, P" uniqKey="Chenal P" first="P" last="Chenal">P. Chenal</name>
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<term>Humans</term>
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<front><div type="abstract" xml:lang="en">We report the case of an 11-year-old child with cystic fibrosis where Geosmithia argillacea has been isolated from sputum. This is a filamentous fungus (mold) recently described as emergent infectious agent in cystic fibrosis patients. In our case, the presence of G. argillacea was not associated with clinical disorder. However, recent evidence shows that it can be responsible for very serious invasive infection, especially in chronic granulomatous disease and may be, after lung transplantation.</div>
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<Title>Journal de mycologie medicale</Title>
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<ArticleTitle>[Isolation of Geosmithia argillacea in a cystic fibrosis patient].</ArticleTitle>
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<Abstract><AbstractText>We report the case of an 11-year-old child with cystic fibrosis where Geosmithia argillacea has been isolated from sputum. This is a filamentous fungus (mold) recently described as emergent infectious agent in cystic fibrosis patients. In our case, the presence of G. argillacea was not associated with clinical disorder. However, recent evidence shows that it can be responsible for very serious invasive infection, especially in chronic granulomatous disease and may be, after lung transplantation.</AbstractText>
<CopyrightInformation>Copyright © 2013 Elsevier Masson SAS. All rights reserved.</CopyrightInformation>
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<VernacularTitle>Isolement de Geosmithia argillacea chez un enfant atteint de mucoviscidose.</VernacularTitle>
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<KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="N">Cystic fibrosis</Keyword>
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<Keyword MajorTopicYN="N">Geosmithia argillacea</Keyword>
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<Keyword MajorTopicYN="N">Mycoses en pédiatrie</Keyword>
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