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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
1997-10-14
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pubmed:abstractText |
We recently reported partially to wholly reversible hypertrophic cardiomyopathy, including severe hypertrophic obstructive cardiomyopathy, as a side effect in pediatric transplant recipients receiving tacrolimus immunosuppression. This seemed to be dose related. We describe a pediatric patient receiving tacrolimus who died 3 weeks after liver/bowel transplantation. Postmortem findings revealed arteritis of cardiac arteries and extensive calcification of cardiac tissue suggesting a possible mechanism of tacrolimus cardiac toxicity. This is consistent with recent reports of tacrolimus increasing calcium release into the sarcoplasmic reticulum of cardiac and striated muscle.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
0041-1337
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
15
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pubmed:volume |
64
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
773-5
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:9311719-Arteritis,
pubmed-meshheading:9311719-Calcium,
pubmed-meshheading:9311719-Cardiomyopathy, Hypertrophic,
pubmed-meshheading:9311719-Carrier Proteins,
pubmed-meshheading:9311719-Child, Preschool,
pubmed-meshheading:9311719-Humans,
pubmed-meshheading:9311719-Immunosuppressive Agents,
pubmed-meshheading:9311719-Intestine, Small,
pubmed-meshheading:9311719-Liver Transplantation,
pubmed-meshheading:9311719-Male,
pubmed-meshheading:9311719-Sarcoplasmic Reticulum,
pubmed-meshheading:9311719-Tacrolimus,
pubmed-meshheading:9311719-Transplantation, Homologous
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pubmed:year |
1997
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pubmed:articleTitle |
Arteritis and increased intracellular calcium as a possible mechanism for tacrolimus-related cardiac toxicity in a pediatric transplant recipient.
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pubmed:affiliation |
Department of Paediatrics, Children's Hospital of Western Ontario, University of Western Ontario, London, Canada.
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pubmed:publicationType |
Journal Article,
Case Reports
|