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Albornoz Carlos E

Maternity Hospital San Roque, Argentina

Title: Congenital Oropharyngeal Teratoma, a rare pathology a serious complication at birth

Abstract

Oropharyngeal teratomas arise from the base of the skull or the posterior wall of the skull. Pharynx and extend inferiorly causing partial or complete obstruction of the
tract air and digestive, so prenatal diagnosis is important to establish a treatment plan, appropriate and immediate management and improve the survival of newborns. The most frequent teratomas are sacrococcygeal (45 to 65%), gonads (10 to 35%), anterior mediastinum (10 to 12%), retroperitoneum (3 to 5%), cervical (3 to 6%),
presacral (3 to 5%), nervous system (2 to 4%) and less than 2% are oropharyngeal. The prevalence in women is 3:1. The objective of this work is to present and describe the clinical case of a patient who was diagnosed with this pathology at our medical institution. Awareness of work groups that rapid coordination and team effort leads to a successful outcome of a rare and uncommon pathology that can lead to death.

Biography

To be updated