Hypermucoviscous Klebsiella Syndrome Without Liver Abscess in a Patient With Immunoglobulin G2 Immune Deficiency
Author(s) -
Asim Alsaedi,
Amber Janower,
JannTay Wang,
Kim Nichol,
James A. Karlowsky,
Pamela Orr,
Yoav Keynan
Publication year - 2014
Publication title -
open forum infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.546
H-Index - 35
ISSN - 2328-8957
DOI - 10.1093/ofid/ofu080
Subject(s) - medicine , liver abscess , bacteremia , antibody , common variable immunodeficiency , meningitis , immunodeficiency , pyogenic liver abscess , immunology , klebsiella pneumoniae , brain abscess , immune system , abscess , microbiology and biotechnology , antibiotics , pediatrics , surgery , escherichia coli , biology , gene , biochemistry
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.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.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.To our knowledge, this is the first report of HMVKP associated with predisposing antibody deficiency.
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