JRCD is now an open‑access journal and also accepts high‑quality papers beyond the field of rare cardiovascular diseases and disorders
Journal Title: Journal of Rare Cardiovascular Diseases - Year 2018, Vol 3, Issue 7
Abstract
n/a
Authors and Affiliations
Piotr Podolec
Keywords
Related Articles
- EP ID EP383443
- DOI 10.2041/jrcd.vol3no7.338
- Views 95
- Downloads 0
Partial recovery of left ventricular function in dilated cardiomyopathy as a result of tuberculosis treatment
We present the case of a young patient with dilated cardiomyopathy (DCM) and concomitant pulmonary tuberculosis (TB), emphasising the need for an interdisciplinary approach when considering underlying aetiology. A 36‐yea...
Left atrial myxoma as a cause of multiple cerebral microembolization (RCD code: VI‐1A.1)
We report a case of a 56-year-old female after breast cancer treatment, who was diagnosed with left atrial myxoma as a rare cause of cerebral and cerebellar stroke.JRCD 2017; 3 (5): 168–170
Severe aortic regurgitation and pulmonary hypertension in an 18‑year‑old patient after balloon aortic valvuloplasty (RCD code: IV‑5.A2)
Aortic stenosis is the most common form of congenital left ventricle outflow tract obstruction. It may be a life threatening ductal-dependent condition in newborns and necessitating urgent percutaneous balloon aortic val...
45‑year‑old man with hypertrophic cardiomyopathy after alcohol ablation, progression to dilated cardiomyopathy (RCD code: III‑1B.8a)
Hypertrophic cardiomyopathy (HCM) is the most common inheritable cardiac disorder with an estimated prevalence of 1:500 in the general population. In minority of patients, with the prevalence approximately of 3–5%, HCM p...
Giant cell aortitis of the ascending aorta without signs and symptoms of systemic vasculitis
We report a case of a patient with giant cell aortitis – a rare cause of aneurysm of the ascending aorta. Modern imaging techniques show promise in diagnosis, however the diagnosis only after hystopathotological examinat...