The classification and management of salivary gland tumours can be problematic for a variety of reasons. These tumours are not common, and additionally show a very wide range of cell types and morphological configurations between various tumour types, and sometimes even within a single tumour mass. Microscopic interpretation of excision specimens can also be confounded by artefactual changes resulting from the increasing use of pre-operative fine-needle aspiration biopsies. Moreover, the behaviour of many of the tumours is unpredictable. For example, pleomorphic adenoma, the most common salivary gland neoplasm, whilst a benign tumour, has a propensity to recur and also to progress to malignancy. On the other hand, tumours such as acinic cell carcinoma and mucoepidermoid carcinoma, although frankly malignant, can sometimes behave in a relatively lowgrade manner. In the parotid gland, the presence of the facial nerve can cause significant difficulties in both pre-operative diagnosis and surgical excision.For all these reasons, close liaison between the surgical team, histopathologists, radiologists and oncologists is particularly critical to ensure optimal management of patients with these tumours.