Case report
Primary cardiac leiomyosarcoma: imaging with 2-D echocardiography, electron beam CT and 1.5-Tesla MR

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Introduction

Primary cardiac sarcomas are extremely rare [1]. There are only a few case reports concerning the sonography, computed tomography (CT) and magnetic resonance imaging (MRI) appearance of cardiac leiomyosarcoma 2, 3, 4, 5. In a review of the literature reported by Nguyen et al., only 27 cases (including his own patient) of primary leiomyosarcoma of the heart had been reported [2]. Leiomyosarcoma is a highly aggressive and local invasive tumor with mean survival of 6 months from the time of diagnosis, if the patient was not treated [3]. We present a case of pathologically proved left atrium leiomyosarcoma who received 2-dimensional (2-D) echocardiography, electron beam CT (EBCT) scan and cardiac MRI.

Section snippets

Case report

A 28-year-old lady was admitted in September, 1995 via the emergency room with the chief complaint of intermittent fever for about 2 months. She also had body weight loss, poor appetite and anemia. The patient had no past history of hypertension, tuberculosis, hepatitis or previous surgery. There was no exertional dyspnea, no night sweating, no cough and no chest tightness.

Physical examination on admission revealed anemic conjunctiva and clubbing fingers on both hands. A grade II diastolic

Discussion

Malignant primary cardiac tumors are extremely rare, approximately 16–40 times less common than secondary cardiac tumors. Most of the primary cardiac malignancies are sarcomas and the leiomyosarcomas are among the rarest ones 1, 2, 3, 6, 7. The estimated incidence of primary cardiac leiomyosarcoma is less than 0.25% of all cardiac tumors and 1% of all primary cardiac malignant lesions 3, 6. Many cardiac sarcomas arise from the right atrium 1, 5, 7, 8. According to Nguyen et al., 27 cases of

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