Ultraschall in Med 2012; 33(1): 85-86
DOI: 10.1055/s-0029-1245552
Kasuistik/Case Report

© Georg Thieme Verlag KG Stuttgart · New York

Prenatal Ultrasound Diagnosis of a Multiple Atypical Right Atrial Cardiac Fibroma

Pränatale sonografische Diagnose eines multiplen atypischen rechts-atrialen FibromsL. B. Colmorn, T. Jensen, B. L. Petersen, M. Helvind, F. S. Jørgensen
Further Information

Publication History

received: 17.2.2010

accepted: 1.6.2010

Publication Date:
16 December 2010 (eFirst)

Introduction

Congenital cardiac tumors are very rare with an incidence at birth of approximately 0.0017 – 0.28 % (Holly DG et al. J Am Coll Cardiol 1995; 26: 516 – 520). The majority of cardiac tumors in children are benign, with only approximately 10 % being malignant. The manifestations of a cardiac tumor in fetal life include congestive heart failure, arrhythmias, hydrops and sudden death (Allan L. In Textbook of Fetal Cardiology: Greenwich Medical Media, London, 2000; 358 – 365; Atallah J et al. Pediatr Cardiol 2006; 27: 493 – 496).

We report a case with an atypical form of cardiac fibroma located in the right atrium. To the best of our knowledge a cardiac fibroma located in the right atrium has not previously been reported in the literature. The prenatal diagnosis was made at 36 weeks of gestation.

1 VVI is a pacemaker that senses and stimulates in the ventricle alone and is inhibited by spontaneous electrical activity in the ventricle.

Miss Lotte Berdiin Colmorn

Gynecology and obstetrics, Hvidovre University Hospital

Kettegaard Allé 30

DK-2650, 2650 Hvidovre, Denmark

Phone: ++ 3 63 23 63 2

Fax: ++ 3 63 23 36 1

Email: colmorn@dadlnet.dk