Title of article :
“Benign Tumor with Perivascular Myoid Differentiation”, A Rare Yet Interesting Case Report in a Nine-Month-Old Infant
Author/Authors :
Mozaffari, Kambiz MD - Associate Professor of Pathology Rajaie Cardiovascular Medical and Research Center - Iran University of Medical Sciences, Tehran , Moradian, Maryam MD - Assistant Professor of Pediatric Cardiology - Rajaie Cardiovascular Medical and Research Center - Iran University of Medical Sciences, Tehran , Baharestani, Bahador MD - Assistant Professor of Cardiac Surgery - Rajaie Cardiovascular Medical and Research Center - Iran University of Medical Sciences, Tehran , Mortezaeian, Hojjat MD - Associate Professor of Pediatric Cardiology - Cardiovascular Intervention Research Center - Rajaie Cardiovascular Medical and Research Center - Iran University of Medical Sciences, Tehran , Bakhshandeh, Hooman MD - PhD. Associate Professor of Epidemiology - Rajaie Cardiovascular Medical and Research Center - Iran University of Medical Sciences, Tehran
Abstract :
Introduction: Heart tumors in children are very rare, however in case of presence, they may cause significant morbidity.
Case Report: We present a nine-month-old female infant who was admitted to the emergency ward due to severe tachypnea.
Echocardiography showed a huge echogenic mass in the right atrium occupying almost half of its cavity. It was originated from
the roof of RA and would herniate to the right ventricle during diastole causing tricuspid valve stenosis. The excised specimen was
similar to a cardiac myxoma. Microscopically, a myxoid background was seen with foci of spindle cell proliferation. Further study
of the tumor showed that it was of smooth muscle origin. After nine months of follow-up from the surgery date, she was healthy.
Conclusions: Considering benign nature of the tumor and its derivation from smooth muscle, it is appropriate to designate it
“Benign Tumor with Perivascular myoid differentiation”. This is a rare, interesting entity which conforms to our findings.
Keywords :
Heart Neoplasms , Infant , Rare Diseases , Pediatric
Journal title :
Multidisciplinary Cardiovascular Annals