Validation of the Milan system for reporting salivary gland cytopathology: a single institution's 10-year experience

J Am Soc Cytopathol. 2022 Sep-Oct;11(5):264-273. doi: 10.1016/j.jasc.2022.05.001. Epub 2022 May 11.

Abstract

Introduction: Fine needle aspiration cytology is often used for the initial diagnosis and management of patients with salivary gland tumors. Because of its global usage, a consensus classification schema was devised in 2018 to initiate universal reporting of salivary gland cytology specimens, termed the Milan system for reporting salivary gland cytopathology (MSRSGC) and composed of distinct diagnostic categories. Few retrospective studies have been undertaken to review the MSRSGC within institutions.

Materials and methods: We analyzed salivary gland fine needle aspirations during a 10-year span from 2011 to 2021, categorized each cytology case to fit the MSRSGC, and subsequently reviewed the corresponding surgical resections, if indicated, to determine the rate of malignancy (ROM) and rate of neoplasia.

Results: Our ROM was higher (>10%) for the following MSRSGC categories: non-neoplastic, atypia of undetermined significance, and suspicious for malignancy. Also, our data correlated well with the following MSRSGC categories: nondiagnostic, neoplasm-benign, salivary gland neoplasm of uncertain malignant, and malignant.

Conclusions: Although the data were indicative of the ROM for surgically resected salivary gland lesions, the ROM for non-neoplastic lesions could truly be lower given that most lesions in this category will not undergo surgical resection. Additionally, determination of the rate of neoplasia could a tool that could be used to further guide our clinical colleagues.

Keywords: Fine needle aspiration; Milan system for reporting salivary gland cytopathology; Rate of malignancy; Salivary gland cytopathology; cytology-histology correlation.

MeSH terms

  • Biopsy, Fine-Needle
  • Cytodiagnosis
  • Humans
  • Retrospective Studies
  • Salivary Gland Neoplasms*
  • Salivary Glands*