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Tom 17, Nr 1 (2022)
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Opublikowany online: 2022-02-28

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Eksport do Mediów Społecznościowych

Eksport do Mediów Społecznościowych

Left ventricular non-compaction cardiomyopathy: a rare cause of cardiovascular complaints

Azita Rezaei1, Marcin Gregorczyk1, Agnieszka Ciba-Stemplewska2, Katarzyna Starzyk3, Wioletta Korzeluch4, Michał Spałek56, Beata Wożakowska-Kapłon13
Folia Cardiologica 2022;17(1):62-64.

Streszczenie

20-year-old woman with diagnosed in childhood left ventricular non-compaction (LVNC) cardiomyopathy with coexisting arthrogryposis was admitted to the Department of Cardiology due to atypical chest pain, worsening of exercise tolerance, bendopnea and symptoms of bronchial asthma exacerbation. The electrocardiogram (ECG) showed changes indicative of ischemia, without their dynamics. Inflammatory parameters, BNP (B-type natriuretic peptide), and myocardial necrosis markers were not elevated. Systolic and diastolic function on echocardiography (ECHO) was assessed as normal. Despite the initially suggestive clinical picture, the correct direction of the differential diagnosis, and consequently the diagnosis, was established after completing the history of comorbidities.

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Referencje

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  4. van Waning JI, Moesker J, Heijsman D, et al. Systematic review of genotype-phenotype correlations in noncompaction cardiomyopathy. J Am Heart Assoc. 2019; 8(23): e012993.
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