Key result
Surgical repair of the atrial septal defect and biopsy of the unresectable cardiac epicardium hemangioma resulted in the patient remaining asymptomatic with unchanged tumor size over a two-year follow-up.
Why the study?
Cardiac epicardium hemangiomas are exceedingly rare and can coexist with heart malformations, but such cases are not well documented.
Case Report (n=1)
No
This case report describes a rare coexistence of a cardiac epicardium hemangioma and an atrial septal defect, demonstrating that mass biopsy is a viable option when resection is impossible and hemodynamic impairment is absent.
BACKGROUND: Cardiac epicardium hemangiomas are exceedingly rare; however, they can cause significant hemodynamic impairment and large pericardial effusions. On rare occasion, cardiac tumors coexist with malformations of the heart. CASE PRESENTATION: We present the case of a 10-month-old female infant with a rare cardiac surface hemangioma coexisting with malformations of the heart. It revealed an atrial septal defect (ASD) coexisting with an abnormal occupying lesion with high echogenicity. It was 35*12*9 mm in size and was found in the anterior atrioventricular junction to the posterior atrioventricular junction at the bottom of the ventricular septum by transthoracic echocardiography. We performed surgical treatment of the atrial septal defect and performed biopsy with the occupying lesion. The histopathological examination reported a benign tumor as hemangioma. As far as we know, this is the first case in which cardiac surface hemangioma was found to coexist with an atrial septal defect. CONCLUSIONS: Cardiac epicardium hemangiomas is a rare solid tumor of the heart. If the mass is impossible to resect and does not cause hemodynamic impairment, only mass biopsy is possible.
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Chen et al. (2022) conducted a case report in Atrial septal defect and cardiac epicardium hemangioma (n=1). Surgical repair of atrial septal defect and tumor biopsy was evaluated on Symptom resolution and tumor size. Surgical repair of the atrial septal defect and biopsy of the unresectable cardiac epicardium hemangioma resulted in the patient remaining asymptomatic with unchanged tumor size over a two-year follow-up.
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