Author:
Nazir Tahir,Ahmed Saad,Ahmed Irfan Munir
Abstract
Primary cardiac tumours are exceedingly rare in clinical practice and a myxoma is certainly not the first suspected diagnosis on a list of differentials in a patient presenting with breathlessness and tachycardia. Naturally, a structured work-up to rule out much more common conditions will take place. Nonetheless, an index of clinical suspicion is required especially when a clear-cut diagnosis is not forthcoming. We describe a case of a postpartum woman who presented with shortness of breath and palpitations, and was eventually diagnosed with a left atrial tumour. She underwent a successful surgical excision of the mass which was found to be a myxoma on histological examination. We review and present an up-to-date literature review on epidemiology, pathophysiology, clinical features, diagnosis and treatment options for cardiac myxomas.
Reference24 articles.
1. Primary cardiac tumors;Silverman;Ann Surg,1980
2. Cardiac myxomas: results of 14 years' experience;Livi;Thorac Cardiovasc Surg,1984
3. Familial cardiac myxoma: Carney’s complex;Mahilmaran;Tex Heart Inst J,2003
4. Primary cardiac tumors—French studies of 533 cases;Blondeau;Thorac Cardiovasc Surg,1990
5. Carney complex: an update;Correa;Eur J Endocrinol,2015