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Left ventricular clefts - incidental finding or pathologic sign of Wilson's disease?
Zhang, Kun; Reuner, Ulrike; Weidauer, Marie; Speiser, Uwe; Ibrahim, Karim; Christoph, Marian; Heinzel, Frank R; Pieske, Burkert; Heidrich, Felix M; Quick, Silvio.
Afiliação
  • Zhang K; Department of Internal Medicine and Cardiology, Charité - Universitätsmedizin Berlin, Campus Virchow-Klinikum, Augustenburger Platz 1, 13353, Berlin, Germany. kun.zhang@charite.de.
  • Reuner U; Berlin Institute of Health (BIH), Berlin, Germany. kun.zhang@charite.de.
  • Weidauer M; DZHK (German Centre for Cardiovascular Research), partner site Berlin, Berlin, Germany. kun.zhang@charite.de.
  • Speiser U; Department of Neurology, Technische Universität Dresden, University Hospital, Dresden, Germany.
  • Ibrahim K; Technische Universität Dresden, Heart Center, University Hospital, Clinic of Internal Medicine and Cardiology, Dresden, Germany.
  • Christoph M; Technische Universität Dresden, Heart Center, University Hospital, Clinic of Internal Medicine and Cardiology, Dresden, Germany.
  • Heinzel FR; Department of Cardiology, Technische Universität Dresden, Klinikum Chemnitz, Chemnitz, Germany.
  • Pieske B; Department of Cardiology, Technische Universität Dresden, Klinikum Chemnitz, Chemnitz, Germany.
  • Heidrich FM; Department of Internal Medicine and Cardiology, Charité - Universitätsmedizin Berlin, Campus Virchow-Klinikum, Augustenburger Platz 1, 13353, Berlin, Germany.
  • Quick S; DZHK (German Centre for Cardiovascular Research), partner site Berlin, Berlin, Germany.
Orphanet J Rare Dis ; 14(1): 244, 2019 11 07.
Article em En | MEDLINE | ID: mdl-31699127
ABSTRACT

BACKGROUND:

Wilson's disease is an inherited autosomal recessive multi-systemic disorder characterized by reduced excretion and consequently excessive accumulation of copper in different organs, such as the heart.

RESULTS:

In a prospective controlled trial, which is the largest to date, we evaluated 61 patients with Wilson's disease, age- and sex-matched to 61 healthy patients, for cardiac manifestation using cardiac magnetic resonance imaging. Patients were under stable disease and had no signs of heart failure at the time of examination. We detected a left ventricular cleft, an invagination penetrating more than 50% wall thickness of the adjoining compact myocardium in diastole, in 20% of the patients (12 out of 61) compared to 5% among control patients (3 out of 61, p = 0.013). No correlation between the incidence of cleft and a certain genotype of Wilson's disease was found. All described cases were incidental findings and none of the patients showed other signs of cardiac involvement.

CONCLUSIONS:

To conclude, the results of this study suggests that the increased occurrence of left ventricular clefts is due to Wilson's disease. Large studies with a long observation period are needed for further evaluation.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ventrículos do Coração / Degeneração Hepatolenticular Tipo de estudo: Clinical_trials / Diagnostic_studies / Observational_studies / Risk_factors_studies Limite: Female / Humans / Male Idioma: En Revista: Orphanet J Rare Dis Assunto da revista: MEDICINA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Alemanha

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Ventrículos do Coração / Degeneração Hepatolenticular Tipo de estudo: Clinical_trials / Diagnostic_studies / Observational_studies / Risk_factors_studies Limite: Female / Humans / Male Idioma: En Revista: Orphanet J Rare Dis Assunto da revista: MEDICINA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Alemanha