(Circulation. 1999;99:e1-e2.)
© 1999 American Heart Association, Inc.
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From the Divisions of Pediatric Cardiology and Cardiothoracic Surgery, The Ohio State University, Children's Hospital, Columbus, Ohio.
Correspondence to Curt J. Daniels, MD, Columbus Children's Hospital, Division of Cardiology, 700 Children's Dr, Columbus, OH 43205. E-mail cdaniels@chi.osu.edu
A17-year-old gravida II,
para I woman was referred for a fetal echocardiographic
evaluation at 28 weeks of gestation because of the finding of hydrops
fetalis on an obstetrical scan. The study demonstrated a large,
complex, anterior mediastinal mass resulting in rotation of the heart
leftward and posterior with compression of the right heart chambers
(Figure 1
). The intracardiac
anatomy was normal, with no significant inflow or outflow
obstruction identified. Intrauterine removal of the mass was considered
but declined by the parents. Preterm labor developed at 32 weeks of
gestation and was unresponsive to medical management. The infant was
delivered by cesarean section and required immediate endotracheal
intubation for respiratory distress. The infant developed hypotension
responsive to volume resuscitation and vasopressor medications. The
infant's respiratory status stabilized with high-frequency
ventilation.
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An MRI was obtained to evaluate the mass and its extent within the
thoracic cavity before surgical intervention. The MRI confirmed the
diagnosis of a large anterior mediastinal mass consistent with
a pericardial teratoma (Figure 2
).
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