Epignathus: Difference between revisions

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Revision as of 10:56, 17 March 2025

Epignathus is a rare type of oropharyngeal teratoma, a tumor that develops in the oral cavity of a fetus. This condition is often associated with a high rate of mortality due to airway obstruction and polyhydramnios.

Overview

Epignathus is a rare congenital malformation that is characterized by a complex, often large, oropharyngeal teratoma. It is a type of teratoma, a tumor made up of several different types of tissue, such as hair, muscle, teeth, or bone. These tumors typically develop in the oral cavity and can extend into the nasopharynx, skull base, or neck.

Etiology

The exact cause of epignathus is unknown. However, it is thought to be related to errors during the development of the placenta. Some studies suggest a possible association with maternal use of certain medications during pregnancy, but more research is needed to confirm these findings.

Diagnosis

Diagnosis of epignathus is usually made during a routine ultrasound examination during pregnancy. The tumor can often be seen as a mass in the oral cavity of the fetus. In some cases, the diagnosis may not be made until after birth.

Treatment

Treatment for epignathus often involves surgery to remove the tumor. In some cases, surgery may be performed while the baby is still in the womb. This is known as fetal surgery. Other treatments may include chemotherapy or radiation therapy, depending on the specific characteristics of the tumor.

Prognosis

The prognosis for babies with epignathus is often poor. Many babies with this condition die before birth or shortly after due to complications such as airway obstruction or polyhydramnios. However, with early diagnosis and treatment, some babies with epignathus can survive and have a good quality of life.

See also

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