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Published on: May 16, 2015
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Epignathus in the neonatal period: an unexpected finding
María Erroz Ferrer1,2, Asier Oliver Olid3,4, Sara Mesa Helguera3
1Pediatric Service, University Hospital of Navarra, Calle Irunlarrea 3, Pamplona, Navarra, 31008, Spain. merroz@alumni.unav.es.
Summary
Epignathus, a rare congenital teratoma, can cause severe airway obstruction in newborns. Early multidisciplinary intervention and surgical tumor resection are crucial for favorable outcomes in affected infants.
Area of Science:
- Congenital Malformations
- Pediatric Surgery
- Neonatal Medicine
Background:
- Epignathus is a rare congenital teratoma presenting a significant risk of neonatal upper airway obstruction.
- This case report details a full-term neonate diagnosed with epignathus without prior prenatal detection.
Purpose of the Study:
- To highlight the critical importance of early, multidisciplinary intervention in managing epignathus.
- To present an updated review of epignathus, emphasizing its association with airway compromise.
Main Methods:
- A case report of a neonate with epignathus presenting with severe respiratory distress at birth.
- Diagnostic imaging, blood tumor markers (alpha-fetoprotein), and histopathological analysis were utilized.
- Surgical resection of the teratoma was performed on day five, with subsequent positive pressure ventilation.
Main Results:
- The neonate presented with severe airway obstruction due to a hard palate tumor and cleft palate.
- Diagnostic imaging revealed a teratoma with dental structures; elevated alpha-fetoprotein supported the diagnosis.
- Histopathology confirmed the tumor as a teratoma, and the infant showed favorable clinical progress post-surgery.
Conclusions:
- Epignathus poses a high risk of neonatal mortality primarily due to airway obstruction.
- Prompt multidisciplinary intervention and surgical management are vital for improving patient outcomes.
- This case underscores the need for awareness and timely management of congenital teratomas like epignathus.

