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Abnormal troponin I levels in a thalassemia major patient with high ferritin concentration, permanent atrial fibrillation and without acute coronary syndrome
- Source :
- International Journal of Cardiology. 138:e24-e27
- Publication Year :
- 2010
- Publisher :
- Elsevier BV, 2010.
-
Abstract
- Thalassemia is a congenital hemoglobinopathy leading to anemia because of impaired erythropoiesis and peripheral hemolysis. Thalassemia major patients are transfusion dependent and it results in iron accumulation. The heart is one of the major organs affected with iron overload and iron induced cardiac dysfunction (pump and conduction abnormalities) remains the number one cause of death among thalassemia major patients. It has been reported that a high ferritin concentration is related to high troponin levels in hemodialysis patients receiving more intravenous iron sucrose. Abnormal troponin I levels have also been reported without acute coronary syndrome. We present a case of abnormal troponin I levels in Thalassemia major patient with high ferritin concentration, permanent atrial fibrillation and without acute coronary syndrome. To our knowledge, this is the first report of abnormal troponin I levels in a Thalassemia major patient with high ferritin concentration and without acute coronary syndrome and also this case focuses attention on the importance of the correct evaluation of abnormal troponin I levels.
- Subjects :
- Male
medicine.medical_specialty
Acute coronary syndrome
Anemia
Thalassemia
Electrocardiography
hemic and lymphatic diseases
Internal medicine
Atrial Fibrillation
Troponin I
Humans
Medicine
Acute Coronary Syndrome
biology
business.industry
beta-Thalassemia
Beta thalassemia
Middle Aged
medicine.disease
Troponin
Ferritin
Hemoglobinopathy
Echocardiography
Ferritins
Cardiology
biology.protein
Cardiology and Cardiovascular Medicine
business
Subjects
Details
- ISSN :
- 01675273
- Volume :
- 138
- Database :
- OpenAIRE
- Journal :
- International Journal of Cardiology
- Accession number :
- edsair.doi.dedup.....3ebf215c965ee3502585020d497ef018
- Full Text :
- https://doi.org/10.1016/j.ijcard.2008.06.039