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Obstructing Nasopharyngeal Teratoma in the NeonateA 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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