A rare case of ameloblastic carcinoma | Ear, Nose & Throat Journal Skip to content Skip to navigation

A rare case of ameloblastic carcinoma

| Reprints
September 18, 2014
by Michael Yunaev, MBBS; Muzib Abdul-Razak, FRCS(Edin); Hedley Coleman, FFOP(RCPA); Yaroslav Mayorchak, MBBS; Ian Kalnins, FRACS


Ameloblastic carcinoma is a rare type of ameloblastoma that has received little mention in the literature. While a number of cases have been published over many years, no institution has been able to produce a substantial case series. Ameloblastic carcinoma originates in the embryonic tooth components. It is believed to be an aggressive tumor that can metastasize; once metastasis occurs, the prognosis tends to be poor. Ameloblastic carcinoma is primarily a surgical condition that is best treated with resection; there has been little indication that other modalities are helpful. We present the case of a 40-year-old woman who was found to have a mandibular lesion by a dentist. After surgical resection, the tumor was found to be an ameloblastic carcinoma. The patient recovered without complication, and she was recurrence-free 18 months postoperatively. We also briefly review the available literature on the natural history of and management options for this rare tumor.

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