Fine needle aspiration cytology of polymorphous adenocarcinoma of the salivary glands: A report of 11 patients and review of the literature

• Published in: Diagnostic cytopathology 2020-11, Vol.48 (11), p.1013-1020
• Main Authors: Jiménez‐Heffernan, José A., Rodríguez‐García, Ana M., González‐Peramato, Pilar, López‐Ferrer, Pilar, Muñoz‐Hernández, Patricia, Gordillo, Carlos H., Viguer, José M., Vicandi, Blanca
• Format: Article
• Language: English
• Subjects: cytology; fine needle aspiration; Kinases; polymorphous adenocarcinoma; salivary glands; Tumors
• ISSN: 8755-1039; 1097-0339
• DOI: 10.1002/dc.24473

Background Polymorphous adenocarcinoma (PAC) is a rare malignant tumor of the minor salivary glands. It has an infiltrative growth, variable architectural patterns, neurotropism and cellular monomorphism. Approximately 75% of the cases show a specific mutation in the protein kinase D1 (PRKD1) gene. Reflecting the rarity of the tumor and intraoral location, the cytologic experience is limited with few reported series. In this study we analyze our cytologic experience to determine if a preoperative diagnosis is possible. Methods A retrospective study of 11 patients with PAC in which a cytologic study was available. A review of the literature was also performed. Results Our study shows that PAC has relatively constant cytological features. The analysis of the cytological literature although it shows some heterogeneity, also reveals repetitive cytological findings. Smears are cellular with irregular groups some showing pseudopapillary branching morphology. Monolayered clusters and small acinar structures are also present. Most cases have small metachromatic globules embedded within the groups determining a cylindromatous pattern. Tumoral cells are small and uniform with scarce to moderate cytoplasm. Nuclei are round and oval with occasional grooves and small nucleoli. Conclusion PAC has characteristic cytological features that together with its location in minor salivary gland must make us consider it preoperatively. It may resemble basal cell adenoma and epithelial‐rich pleomorphic adenoma so we should be cautious in the final diagnosis. Whenever possible, the characteristic cytomorphology of PCA should make us evaluate the mutational status of PRKD1 gene since it may permit a more accurate diagnosis.