Objective: To perform a retrospective investigation of our institutional experience with salivary gland fine needle aspirations (FNA) through the framework of The Milan System for Reporting Salivary Gland Cytopathology (MSRSGC) and assess the risks of neoplasm and malignancy for each diagnostic category.were retrospectively categorised according to the MSRSGC. When available, preoperative cytological results were correlated with subsequent histological follow-up.
Results: In total, 893 FNAs were reviewed. The specimens were retrospectively classified as nondiagnostic (ND: 13.5%), non-neoplastic (NN: 16.1%), atypia of undetermined significance (AUS: 10.8%), benign neoplasm (BN: 34.9%), salivary gland neoplasm of uncertain malignant potential (SUMP: 8.2%), suspicious for malignancy (SM: 2.7%) and malignant (M: 13.8%). Histological follow-up was available for 429 cases (48%); the majority (68.1%) were benign. The risks of neoplasm and malignancy for each category were as follows: ND: 64.5%, 16.1%; NN: 42.9%, 17.9%; AUS: 79.6%, 30.6%; BN: 100%, 2.2%; SUMP: 100%, 46.6%; SM: 94.7%, 78.9%; and M: 100%, 98.5%. Conclusions: The MSRSGC is a useful classification scheme for stratifying salivary gland lesions according to their associated risk of malignancy and guiding clinicians toward appropriate management. Diagnostic pitfalls are seen in a small proportion of cases and a multidisciplinary approach for assessing salivary gland pathology is essential in their evaluation. K E Y W O R D S cytology, fine needle aspiration, Milan system, risk of malignancy, salivary gland 1 | INTRODUCTION Fine needle aspiration (FNA) is a well established, cost-effective, and minimally invasive diagnostic tool for sampling salivary gland lesions. 1,2FNA cytology can be useful for distinguishing between non-neoplastic and neoplastic entities. 3 However, due to intratumoral heterogeneity and frequent overlapping cytomorphological features between many tumours, precise subtyping of neoplasms can be challenging. 4-7 This distinction is important as the treatment options vary across the spectrum of salivary gland pathologies. Non-neoplastic lesions can be managed conservatively, whereas a neoplastic diagnosis warrants surgical excision-in most cases with extensive surgery for high-grade malignancies, lymph node dissection for metastases and a haematology-oncology referral for haematological malignancies. Hence, cytological diagnoses that are descriptive without proper categorisation can be confusing for clinicians who need more definitive diagnoses to guide their management decisions. 8Until recently, there has been a lack of a uniform reporting scheme for cataloguing salivary gland lesions. It is in this setting that an international panel of experts under the joint efforts of the American