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dc.contributor.authorAlsaedi, A
dc.contributor.authorJanower, A
dc.contributor.authorWang, JT
dc.contributor.authorNichol, K
dc.contributor.authorKarlowsky, J
dc.contributor.authorOrr, P
dc.contributor.authorKeynan, Y
dc.date.accessioned2015-03-25T08:10:17Z
dc.date.available2015-03-25T08:10:17Z
dc.date.issued2014
dc.identifier.urihttp://hdl.handle.net/11295/81652
dc.description.abstractBACKGROUND: Hypermucoviscous Klebsiella pneumoniae (HMVKP) emerged as a cause of invasive infections in South-East (SE) Asia. It has become the most common cause of liver abscess in that region, and it is a significant causative organism in endogenous endophthalmitis and meningitis. During the past decade, cases of this uniquely virulent organism have been reported outside of SE Asia, with a propensity to affect individuals of SE Asian descent. Cases have been reported from North America including Canada. METHODS: We report a case of a patient of Filipino descent living in Canada who presented with recurrent HMVKP bacteremia in the absence of pyogenic liver abscess or other localized metastatic Klebsiella infection. RESULTS: Investigations identified an immunoglobulin (Ig)G2 deficiency and low IgM indicating potential common variable immunodeficiency, and administration of intravenous immunoglobulins was associated with prevention of further recurrences. CONCLUSIONS: To our knowledge, this is the first report of HMVKP associated with predisposing antibody deficiency.en_US
dc.language.isoenen_US
dc.publisherUniversity of Nairobien_US
dc.subjectIgG2 deficiency; Klebsiella pneumonia; hypermucoviscousen_US
dc.titleHypermucoviscous Klebsiella syndrome without liver abscess in a patient with immunoglobulin g2 immune deficiency.en_US
dc.typeArticleen_US
dc.type.materialen_USen_US


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