Intrapericardial teratomas (IPT) are rare tumors that have been reported to cause severe cardiorespiratory distress in neonates.
1.2 There has been only one case previously diagnosed in utero, which wasscanned in the third trimester, and had no evidence of fetal hydrops. 3 We wish to report a case of an IPT diagnosed in utero in the second trimester that went on to cause severe non~ immune hydrops.
CASE REPORTA 26-week gestation was referred to our Institution for the evaluation of a possible fetal thoracic mas!l. The mother was gravida 3, para 0, abortions 2, with no family history of con· genital disease. Sonographic evaluation demonstrated a breech fetus with growth parameters concordant with 26 weeks. Within the fetal thorax a 5 X 6 mm soft tissue mass was positioned on the rightside of the heart and appeared to con· tain small areas of echogenic foci. It was thought these foci could represent calcifications that were too small to cause acoustic shadowing. The heart was positioned normally within the chest. A large pericardia! effusion was also noted (Fig. 1). The fetal lungs were visualized in the posterior aspect of the thorax. Because the lungs were not surrounded or float·