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Salivary gland tumors: Epidemiology, pathogenesis, evaluation, and staging

INTRODUCTION

Salivary glands produce and secrete saliva from a glandular structure, the secretory acini, ducts, and myoepithelial and basal cells. Salivary gland tumors (SGTs), which can be benign or malignant (table 1), can arise from either the major salivary glands (parotid, submandibular, and sublingual) (figure 1) or the minor salivary glands, which are located throughout the submucosa of the mouth and upper aerodigestive tract, including the oral cavity (especially the palate), paranasal sinuses, larynx, and pharynx [1,2].

The epidemiology, pathogenesis, preoperative evaluation, and staging of salivary gland tumors are presented here. Treatment of salivary gland tumors, for both locoregional and metastatic disease, is discussed separately. (See "Salivary gland tumors: Treatment of locoregional disease" and "Malignant salivary gland tumors: Treatment of recurrent and metastatic disease" and "Pathology of head and neck neoplasms".)

EPIDEMIOLOGY AND PATHOGENESIS

The epidemiology of SGTs is not well documented and varies based upon geography and populations studied. In general, tumors of the salivary gland are relatively rare, comprising 3 to 6 percent of head and neck neoplasms in adults [3].

The factors responsible for salivary gland tumorigenesis are unclear. In comparison to most other head and neck cancers, exposure to tobacco smoke and alcohol intake have not been consistently associated with the development of SGTs, whereas previous radiation exposure appears to be a risk factor for the development of SGTs, particularly mucoepidermoid carcinoma [4-11].

Warthin tumor, in contrast to other SGTs, does have a strong association with smoking. Although this benign tumor has been historically associated with older men, the incidence in women has increased and parallels the increased smoking rates of women [2,12,13].

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