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dc.contributor.authorKashtan, Clifford E.
dc.contributor.authorPrimack, William A.
dc.contributor.authorKainer, Gad
dc.contributor.authorRosenberg, Andrew R.
dc.contributor.authorMcDonald, Ruth A.
dc.contributor.authorWarady, Bradley A.
dc.date2022-08-11T08:10:12.000
dc.date.accessioned2022-08-23T16:59:08Z
dc.date.available2022-08-23T16:59:08Z
dc.date.issued1999-10-01
dc.date.submitted2012-05-02
dc.identifier.citationPediatr Nephrol. 1999 Oct;13(8):678-82. doi:10.1007/s004670050680
dc.identifier.issn0931-041X (Linking)
dc.identifier.doi10.1007/s004670050680
dc.identifier.pmid10502126
dc.identifier.urihttp://hdl.handle.net/20.500.14038/43516
dc.description.abstractEight children with autosomal recessive polycystic kidney disease (ARPKD) and recurrent bacteremia with enteric pathogens are described. Typical clinical features of bacterial cholangitis were absent, although in five patients histological and/or microbiological data indicated that the bacteremic episodes originated in the biliary tree. Bacteremia with enteric pathogens or recurrent culture-negative febrile illness in a child with ARPKD should raise suspicion of cholangitis, even in the absence of typical clinical findings.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=10502126&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1007/s004670050680
dc.subjectBacteremia; Child; Child, Preschool; Cholangitis; Female; Humans; Infant; Intestines; Liver Cirrhosis; Polycystic Kidney, Autosomal Recessive; Recurrence
dc.subjectNephrology
dc.subjectPediatrics
dc.titleRecurrent bacteremia with enteric pathogens in recessive polycystic kidney disease
dc.typeJournal Article
dc.source.journaltitlePediatric nephrology (Berlin, Germany)
dc.source.volume13
dc.source.issue8
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/peds_nephrology/1
dc.identifier.contextkey2816797
html.description.abstract<p>Eight children with autosomal recessive polycystic kidney disease (ARPKD) and recurrent bacteremia with enteric pathogens are described. Typical clinical features of bacterial cholangitis were absent, although in five patients histological and/or microbiological data indicated that the bacteremic episodes originated in the biliary tree. Bacteremia with enteric pathogens or recurrent culture-negative febrile illness in a child with ARPKD should raise suspicion of cholangitis, even in the absence of typical clinical findings.</p>
dc.identifier.submissionpathpeds_nephrology/1
dc.contributor.departmentDepartment of Pediatrics
dc.source.pages678-82


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