Abstract
The most morphologically and clinically varied solid epithelial tumours are salivary gland neoplasms. The current World Health Organization (WHO) classification lists 25 various forms of salivary gland tumours (Table 1). Salivary gland neoplasms exhibit a diversity that is arguably unmatched by any other organ in comparison, notwithstanding their rarity. Less than 4% of all head and neck neoplasms are salivary gland neoplasms, making them rare. The parotid gland is where most salivary gland neoplasms are found, and in adults, 80% of these are benign. Recent years have seen a clearer definition of the cytologic characteristics of salivary gland neoplasms on fine-needle aspiration, making documenting and diagnosis easier. More and more often, salivary gland tumours are found to have genomic abnormalities, such as translocations and gene fusions.
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Nagarkar, N.M., Rao, K.N., Dange, P.S. (2023). Salivary Glands. In: Nagarkar, N.M., Mehta, R., Singh, A., Rao, K.N., Dange, P.S. (eds) Atlas of Head Neck and Skull-base Surgery. Springer, Singapore. https://doi.org/10.1007/978-981-99-6132-0_4
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