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Unexpected high troponin T and I values in a child with hypertrophic cardiomyopathy and acute chest pain: a case report.
van Avezaath, Lisanne K; Nijenhuis, Hessel P; Muller Kobold, Anneke C.
Afiliação
  • van Avezaath LK; Department of Pediatric Cardiology, University of Groningen, Beatrix Children Hospital, University Medical Center Groningen, Groningen, The Netherlands.
  • Nijenhuis HP; Department of Pediatric Cardiology, University of Groningen, Beatrix Children Hospital, University Medical Center Groningen, Groningen, The Netherlands.
  • Muller Kobold AC; Department of Laboratory Medicine, University of Groningen, University Medical Center Groningen, P.O. Box 30.001, 9700 RB Groningen, The Netherlands.
Eur Heart J Case Rep ; 7(8): ytad375, 2023 Aug.
Article em En | MEDLINE | ID: mdl-37575535
Background: Elevated troponin T (cTnT) and/or troponin I (cTnI) can be ascribed to multiple causes, mostly resulting from cardiac tissue damage and in lesser numbers resulting from non-cardiac related causes. The presence of macrotroponins is easily overlooked, with potentially negative consequences. Case summary: This case report presents a case study of a 12-year-old child known to have MYH7 gene-associated hypertrophic cardiomyopathy with acute chest pain combined with an unexpected high cTnT and cTnI. A cardiac cause was deemed unlikely after additional investigation, as these showed no abnormalities. After consulting a laboratory specialist, it could be concluded that the high cTnT and cTnI were a result of macrotroponin complexes, a protein complex consisting of circulating protein and endogenous autoantibodies against that protein, resulting in elevated values with misguiding and uncertain clinical significance. Discussion: Awareness of the existence of macrotroponins could have prevented costly diagnostics and prolonged hospital admission with grave psychological impact, especially in children.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Eur Heart J Case Rep Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Eur Heart J Case Rep Ano de publicação: 2023 Tipo de documento: Article