Iranian Journal of Pediatrics 2011. 21(2):249-252.

Congenital Nasopharyngeal Teratoma in a Neonate
Alireza Mirshemirani, Ahmad Khaleghnejad, Leila Mohajerzadeh, Majid Samsami, Shaghayegh Hasas-yeganeh

Abstract


Background: Congenital germ cell tumors are uncommon. The most common site of teratoma is in the sacrococcygeal region. Teratoma arising from the head and neck comprises less than 10% of reported cases and of these, nasopharyngeal lesions are rare. Teratomas are generally benign, and have a well recognized clinical and histopathological entity. We present a case of nasopharyngeal teratoma (NPT) associated with a wide cleft palate.


Case Presentation: A 20 day old female neonate with a teratoma of the nasopharyngeal area, and wide cleft palate was referred to our center. The protruded mass which measured 6×4×3cm, was of soft consistency, blocked the airway, and prevented oral feeding. Preoperative evaluation and imaging was performed and mass was excised 2 days after admission. Pathology revealed a well-differentiated mature solid teratoma (hairy polyp). The patient had no complication in the post-operative period. Cleft palate was surgically repaired when 2 years old. She is now a six year old girl with normal development.


Conclusion: Congenital nasopharyngeal teratomas are usually benign. Surgery is the treatment of choice, and should be undertaken on an urgent basis, especially in a patient who presents with signs and symptoms of airway obstruction.


Keywords


Teratoma, Nasopharyngeal Tumor, Cleft Palate, Neonate, Airway Obstruction,

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