Key result
Multidisciplinary care with fetal pericardiocentesis and resection successfully treats immature intrapericardial teratoma.
Why the study?
Intrapericardial teratoma is a rare cardiac tumor in fetuses and newborns that can cause life-threatening complications, and early diagnosis and surgery improve survival.
Case Report (n=1)
Highlights the importance of early antenatal diagnosis and a multidisciplinary team approach for the successful management of life-threatening foetal intrapericardial teratoma.
Case report of fetal intrapericardial teratoma supports early intervention where feasible; leaves open need for registry data to guide practice.
Intrapericardial teratoma is a germ-cell tumor that typically arises from the base of the heart. This rare cardiac tumour is the second most common tumor diagnosed in fetuses and newborn. Although benign, it can be massive in size causing direct compression on the heart and associated with significant pericardial effusion resulting life-threatening complications such as cardiac tamponade, heart failure, foetal hydrops, and sudden death. Early antenatal diagnosis and surgical intervention improve the survival. We present a case of immature intrapericardial teratoma diagnosed at 25 weeks of gestation but required multiple foetal pericardiocentesis and premature delivery due to massive pericardial effusion. The importance of multidisciplinary team approach to ensure successful management was highlighted in this case report.
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Mazalan et al. (2022) conducted a case report in Immature intrapericardial teratoma (n=1). Fetal pericardiocentesis, premature delivery, and surgical resection was evaluated. Multidisciplinary management, including fetal pericardiocentesis, premature delivery, and surgical resection, successfully treated a premature neonate with an immature intrapericardial teratoma.
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