[Skip to Content]
Access to paid content on this site is currently suspended due to excessive activity being detected from your IP address 34.204.202.44. Please contact the publisher to request reinstatement.
[Skip to Content Landing]
Article
March 1966

Intranasal Neuroglial Heterotopia: So-Called Nasal Glioma

Author Affiliations

FORT CAMPBELL, KY
From the otolaryngology, pathology, and pediatric services, US Army Hospital, Fort Campbell, Ky. Dr. Strauss is now in private practice in Englewood, NJ.

Am J Dis Child. 1966;111(3):317-320. doi:10.1001/archpedi.1966.02090060127019
Abstract

THE DIFFERENTIAL diagnosis of intranasal masses in children includes a long list of infrequently encountered lesions once nasal polyp is excluded from consideration. The list includes cysts (sebaceous, dermoid, epidermoid, ethmoid, and those of the lacrimal duct apparatus) which are of ectodermal origin, as are nasal polyps. In addition, tumors of mesodermal origin such as hemangioma and lipoma may occur. Neurogenic tumors are occasionally found, ie, meningocele, encephalocele, neurofibroma, and nasal glioma. Finally, teratoma and abscesses should be included.1

Congenital intranasal neuroglial heterotopia, commonly referred to as nasal glioma, presented in a 5-year-old boy. The lesion, masquerading as a nasal polyp, is the subject of this report.

Report of Case  A 5-year-old white boy was referred to the Otolaryngology Service, US Army Hospital at Fort Campbell for evaluation of an intranasal mass obstructing the right nasal chamber. The mass had first been noted seven months earlier and had been

×