Myxoma of the heart (RCD code: VI-1A.1)

Journal Title: Journal of Rare Cardiovascular Diseases - Year 2013, Vol 1, Issue 4

Abstract

Myxomas are the most common primary benign intracardiac tumors. Typically they locate in the left atrium (LA) or right atrium (RA) and are composed of cells, that originate from multipotent mesenchyme. The clinical manifestations of myxomas depend on the anatomic location of the tumor, its size, as well as its mobility. We present two case reports that concern the management of myxoma. The first diagnostic approach for assessment of the myxomas is two dimensional echocardiography. Computed tomography (CT) and Magnetic Resonance (MR) play especially role in providing diagnostic information useful toward surgical planning. Surgical operation and resection of the myxoma is a definite and curative therapy The risk for recurrence of the myxoma is about 2–5 %. The annual clinical surveillance and echocardiographic assesment is reccomended to all patients who undergo a myxoma operation.. JRCD 2013; 1 (4): 29–32

Authors and Affiliations

Hanna Dziedzic-Oleksy, Monika Komar, Maria Olszowska, Małgorzata Urbańczyk-Zawadzka, Barbara Widlińska, Robert Banyś, Piotr Podolec

Keywords

Related Articles

Genetics and genetic testing in pulmonary arterial hypertension

Pulmonary arterial hypertension (PAH) is a rare disease with a high mortality and complex pathomechanism. Recent studies suggest an important role of genetic factors in the development of PAH. It was shown that patients...

Rhythm disorders and electrocardiographic abnormalities in adult patients with pulmonary arterial hypertension (RCD code: class II)

Cardiac arrhythmias may occur in the course of pulmonary hypertension as a result of structural changes related to pressure overload, myocardial hypertrophy and chamber dilation. Arrhythmias compromise greatly to clinica...

Cardiac manifestations in a two‑generation family with Fabry disease (RCD code: III‑2B.2a)

Fabry disease (FD), which is also called angiokeratoma corporis difusum, ceramide trihexosidosis, and Anderson-Fabry disease, is an X-linked inborn error of metabolism of glycosphingolipid pathway. It is caused by the de...

Patent ductus arteriosus recanalization following its successful surgical closure (RCD code: IV-2B.4)

Patent ductus arteriosus (PDA) is rarely diagnosed late in adult life, and frequently in children as an isolated disorder or complex congenital heart defect. PDA represents an anomaly defined by the communication between...

Isolated right ventricular endomyocardial fibrosis in a young male with chronic myeloid leukemia (RCD code: III‑3F.2)

Endomyocardial fibrosis (EMF) is a rare disease of unknown etiology which is more prevalent in tropical countries. EMF is associated with fibrosis of endomyocardium, involving one or both ventricles. It usually presents...

Download PDF file
  • EP ID EP248138
  • DOI 10.20418/jrcd.vol1no4.69
  • Views 111
  • Downloads 0

How To Cite

Hanna Dziedzic-Oleksy, Monika Komar, Maria Olszowska, Małgorzata Urbańczyk-Zawadzka, Barbara Widlińska, Robert Banyś, Piotr Podolec (2013). Myxoma of the heart (RCD code: VI-1A.1). Journal of Rare Cardiovascular Diseases, 1(4), 163-166. https://europub.co.uk/articles/-A-248138