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  Vol. 117 No. 12, December 1991 TABLE OF CONTENTS
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Obstructing Nasopharyngeal Teratoma in the Neonate

A Report of Two Cases

Leonard P. Rybak, MD, PhD; Michael F. Rapp, MD; Murray D. McGrady, MD; Mary R. Schwartz, MD; Philip W. Myers, MD

Arch Otolaryngol Head Neck Surg. 1991;117(12):1411-1415.


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.

(Arch Otolaryngol Head Neck Surg. 1991;117:1411-1415)



Author Affiliations

Laura Orvidas, MD

From the Departments of Surgery and Pathology, Southern Illinois University School of Medicine and St John's Hospital, Springfield.


Footnotes

Accepted for publication April 15, 1991.

Presented before the American Society of Pediatric Otolaryngology, Toronto, Ontario, May 17-19, 1990.

Reprint requests to Department of Surgery, Division of Otolaryngology, Southern Illinois University School of Medicine, PO Box 19230, Springfield, IL 62794-9230 (Dr Rybak).



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THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Nasopharyngeal teratoma causing airway obstruction in the neonate
Altuntas et al.
BMJ Case Reports 2009;2009:bcr0620080260-bcr0620080260.
ABSTRACT | FULL TEXT  





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