Key result
Simultaneous drainage and resection of infant intrapericardial teratoma achieves uneventful recovery with no recurrence.
Why the study?
Intrapericardial teratoma is an extremely rare mediastinal tumor often complicated by massive pericardial effusion causing heart failure and respiratory distress in early infants.
Case Report (n=1)
Simultaneous surgical drainage and tumor resection can be successfully performed for intrapericardial immature teratoma complicated by massive pericardial effusion in infants.
Answers are grounded in this paper and cite their sources.
Alerts clinicians to rare intrapericardial teratoma in distressed infants; leaves open evidence-based management protocols.
Intrapericardial teratoma is an extremely rare mediastinal teratoma that arises at the junction of the ascending aorta and right atrial appendage. The teratoma is often complicated by massive pericardial effusion that compresses the heart and lungs, leading to heart failure and/or respiratory distress and potentially fatal outcomes in early infants. A 4-month-old boy was referred to our institute with slowly progressive appetite loss and respiratory distress and was diagnosed with intrapericardial teratoma with pericardial effusion. The patient underwent simultaneous surgical drainage of the pericardial effusion and tumor resection. The tumor was pathologically diagnosed as an immature teratoma. The postoperative course was uneventful. He is now being followed up in the outpatient clinic and shows no clinical or radiological signs of recurrence.
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Mori et al. (2020) conducted a case report in Intrapericardial immature teratoma with pericardial effusion (n=1). Simultaneous surgical drainage of the pericardial effusion and tumor resection was evaluated on Postoperative course and recurrence. Simultaneous surgical drainage and tumor resection of an intrapericardial immature teratoma in a 4-month-old boy led to an uneventful recovery with no clinical or radiological signs of recurrence.
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