Shaheed Rajaee Cardiovascular Medical Center, Mellat Park, Vali Asr Avenue, Tehran, Iran.
Abstract
Familial cardiac myxoma is a rare syndrome which constitutes approximately 10% or less of all myxomas. We describe a rare case of a simultaneous left atrial and left ventricular mass in a 35- year-old female who presented to our hospital for the evaluation of recurrent cardiac myxoma. Echocardiography revealed a concurrent left atrial and left ventricular mass. Histological findings after surgery confirmed the diagnosis of myxoma
ESMAEILZADEH M., AKBARZADEH Z., YOUSEFI A., SAFAIE A., RAISI K., SHARIFI F. (2004). 'MULTICENTRIC FAMILIAL CARDIAC MYXOMA', Iranian Heart Journal, 5(1.2), pp. 86-88.
CHICAGO
M. ESMAEILZADEH, Z. AKBARZADEH, A. YOUSEFI, A. SAFAIE, K. RAISI and F. SHARIFI, "MULTICENTRIC FAMILIAL CARDIAC MYXOMA," Iranian Heart Journal, 5 1.2 (2004): 86-88,
VANCOUVER
ESMAEILZADEH M., AKBARZADEH Z., YOUSEFI A., SAFAIE A., RAISI K., SHARIFI F. MULTICENTRIC FAMILIAL CARDIAC MYXOMA. Iranian Heart Journal, 2004; 5(1.2): 86-88.
