Campylobacter fetus Bacteremia Revealed by Cellulitis without Gastrointestinal Symptoms in the Context of Acquired Hypogammaglobulinemia: A Report of Three Cases

Campylobacter fetus bacteremia is rare and occurs mainly in patients with immunosuppression. This infection, which often involves secondary localizations has already been reported in some primary humoral immune deficiencies. We describe three cases of severe infection due to C. fetus with cellulitis...

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Autores principales: Brah, Souleymane, Chiche, Laurent, Brun, Marion, Schleinitz, Nicolas, Harle, Jean-Robert, Durand, Jean-Marc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2011
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3350303/
https://www.ncbi.nlm.nih.gov/pubmed/22606424
http://dx.doi.org/10.1155/2011/628902
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author Brah, Souleymane
Chiche, Laurent
Brun, Marion
Schleinitz, Nicolas
Harle, Jean-Robert
Durand, Jean-Marc
author_facet Brah, Souleymane
Chiche, Laurent
Brun, Marion
Schleinitz, Nicolas
Harle, Jean-Robert
Durand, Jean-Marc
author_sort Brah, Souleymane
collection PubMed
description Campylobacter fetus bacteremia is rare and occurs mainly in patients with immunosuppression. This infection, which often involves secondary localizations has already been reported in some primary humoral immune deficiencies. We describe three cases of severe infection due to C. fetus with cellulitis at presentation, but without any gastrointestinal symptoms, occurring in patients with acquired hypogammaglobulinemia.
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spelling pubmed-33503032012-05-17 Campylobacter fetus Bacteremia Revealed by Cellulitis without Gastrointestinal Symptoms in the Context of Acquired Hypogammaglobulinemia: A Report of Three Cases Brah, Souleymane Chiche, Laurent Brun, Marion Schleinitz, Nicolas Harle, Jean-Robert Durand, Jean-Marc Case Rep Gastrointest Med Case Report Campylobacter fetus bacteremia is rare and occurs mainly in patients with immunosuppression. This infection, which often involves secondary localizations has already been reported in some primary humoral immune deficiencies. We describe three cases of severe infection due to C. fetus with cellulitis at presentation, but without any gastrointestinal symptoms, occurring in patients with acquired hypogammaglobulinemia. Hindawi Publishing Corporation 2011 2011-07-09 /pmc/articles/PMC3350303/ /pubmed/22606424 http://dx.doi.org/10.1155/2011/628902 Text en Copyright © 2011 Souleymane Brah et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Brah, Souleymane
Chiche, Laurent
Brun, Marion
Schleinitz, Nicolas
Harle, Jean-Robert
Durand, Jean-Marc
Campylobacter fetus Bacteremia Revealed by Cellulitis without Gastrointestinal Symptoms in the Context of Acquired Hypogammaglobulinemia: A Report of Three Cases
title Campylobacter fetus Bacteremia Revealed by Cellulitis without Gastrointestinal Symptoms in the Context of Acquired Hypogammaglobulinemia: A Report of Three Cases
title_full Campylobacter fetus Bacteremia Revealed by Cellulitis without Gastrointestinal Symptoms in the Context of Acquired Hypogammaglobulinemia: A Report of Three Cases
title_fullStr Campylobacter fetus Bacteremia Revealed by Cellulitis without Gastrointestinal Symptoms in the Context of Acquired Hypogammaglobulinemia: A Report of Three Cases
title_full_unstemmed Campylobacter fetus Bacteremia Revealed by Cellulitis without Gastrointestinal Symptoms in the Context of Acquired Hypogammaglobulinemia: A Report of Three Cases
title_short Campylobacter fetus Bacteremia Revealed by Cellulitis without Gastrointestinal Symptoms in the Context of Acquired Hypogammaglobulinemia: A Report of Three Cases
title_sort campylobacter fetus bacteremia revealed by cellulitis without gastrointestinal symptoms in the context of acquired hypogammaglobulinemia: a report of three cases
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3350303/
https://www.ncbi.nlm.nih.gov/pubmed/22606424
http://dx.doi.org/10.1155/2011/628902
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