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Salivary gland tumors: Treatment of locoregional disease

Authors
William M Lydiatt, MD
Jeanne M Quivey, MD, FACR
Section Editors
Bruce E Brockstein, MD
David M Brizel, MD
Daniel G Deschler, MD, FACS
Marvin P Fried, MD, FACS
Deputy Editor
Michael E Ross, MD

INTRODUCTION

Salivary gland tumors include a wide range of tumor types, which can be either benign or malignant (table 1). Approximately 85 percent arise in the parotid; the remainder originate in the submandibular, sublingual, and minor salivary glands, which are located throughout the submucosa of the mouth and upper aerodigestive tract (figure 1) [1]. Approximately 25 percent of parotid tumors are malignant, compared with 40 to 45 percent of submandibular gland tumors, 70 to 90 percent of sublingual gland tumors, and 50 to 75 percent of minor salivary gland tumors.

Treatment recommendations are based upon retrospective reviews of clinical experience, and there are almost no data from randomized trials to guide treatment decisions. The published literature predominately focuses on the parotid gland, reflecting the relative frequency of parotid gland tumors compared with tumors at other sites. The treatment of locoregional disease, which includes stages I through IVB (table 2), will be discussed here.

Other topics on salivary gland tumors include:

(See "Salivary gland tumors: Epidemiology, diagnosis, evaluation, and staging".)

(See "Malignant salivary gland tumors: Treatment of recurrent and metastatic disease".)

                    

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Literature review current through: Nov 2016. | This topic last updated: Wed Nov 30 00:00:00 GMT+00:00 2016.
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