Cardiac rhabdomyoma: an antenatal illustration.

To cite: Shukla AK, Reddy AK, Latha A, et al. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/ bcr-2014-209256 DESCRIPTION A 22-year-old primiparous woman was referred for a routine antenatal fetal scan. During the scan multiple intracardiac echogenic tumours were detected at 24 weeks gestation. A smaller mass was visible in the left ventricle while a larger one was seen in the right atrium (figure 1). Subsequent antenatal MRI showed considerably enlarged well-defined masses isointense to the adjoining myocardium in T1-weighted (T1W) and hyperintense in T2W images (figure 2). The rest of the pregnancy remained uneventful and the delivery was normal. Postnatal echocardiography confirmed the above findings. Marginal reduction in the tumour size was seen at the age of 3 years. Antenatal cardiac rhabdomyoma, though rare, is the most common cardiac tumour of benign nature known to occur in infancy and childhood. It was first reported in 1982 by DeVore. It is most frequently seen in antenatal sonography and to a lesser extent on MRI. Multiple rhabdomyomas are almost always associated with tuberous sclerosis (100%) whereas the solitary tumours in 50% of cases. About 90% of cases are detected antenatally at around 20 weeks of gestation. In about 90% of detected cases, they are multiple and intraventricular in location. Atrial involvement is considered to be relatively uncommon and is about 30%. Small masses remain clinically asymptomatic while the larger ones are prone to cause outflow tract obstruction and refractory arrhythmias. Histologically, they are hamartomatous in nature and known to be self-limiting without postnatal proliferation. Subtypes include embryonal, botryoid, alveolar or pleomorphic. Surgical intervention is reserved for cases with outflow tract obstruction and refractory arrhythmias. Some tumours usually undergo complete spontaneous regression by 6 years of age.