Obstructing nasopharyngeal teratoma in the neonate. A report of two cases

Arch Otolaryngol Head Neck Surg. 1991 Dec;117(12):1411-5. doi: 10.1001/archotol.1991.01870240103019.

Abstract

True teratomas of the nasopharynx are rare tumors of the newborn. Surgical resection is the treatment of choice. We describe two patients with this entity. The first patient has undergone follow-up for over 10 years, while the second patient was evaluated with fine-needle aspiration and magnetic resonance imaging. The advantages of these studies and alternate surgical techniques are discussed. Of interest is the fact that both patients may have had central nervous system abnormalities.

Publication types

  • Case Reports

MeSH terms

  • Child
  • Female
  • Follow-Up Studies
  • Humans
  • Infant, Newborn
  • Nasopharyngeal Neoplasms / congenital*
  • Nasopharyngeal Neoplasms / pathology
  • Nasopharyngeal Neoplasms / surgery*
  • Postoperative Complications
  • Teratoma / congenital*
  • Teratoma / pathology
  • Teratoma / surgery*