Acinic cell carcinoma mimicking Warthin's tumor: A diagnostic challenge on fine‐needle cytology

Abstract

The cytologic diagnosis of acinic cell carcinoma (ACC) can be challenging due to its polymorphous appearance and sharing cytomorphologic characteristics with other benign and malignant neoplasms as well as non‐neoplastic diseases, even though various histomorphological aspects of ACC have been documented. We presented a 39‐year‐old female patient applied with right pre‐auricular parotid swelling spreading infra‐auricular region which was gradually increased in size for 3 months. Ultrasonographic examination revealed hypoechoic well‐circumscribed mass with 17 × 22 × 29 mm size. Magnetic resonance imaging revealed intra‐parotid solid lesion with cystic areas, slightly hypointense on T1 and hyperintense on T2 weighted images. The mass was pushing the retromandibular vein medially, still lateral to it in the caudal images, but in dumbbell‐shape spreading through parapharyngeal space in superiorly cranial images. Fine‐needle aspiration cytology was also performed with guidance of ultrasonography. The cytological examination of the lesion was characterized by the predominance of heterogeneous lymphoid cells, clusters of epithelial cells with a variety of cytologic appearances, including granular, transparent, vacuolated, and oncocytic, and the presence of numerous naked nuclei with a protein‐like foamy background. Due to intense lymphocytic inflammation, it was considered as benign primary parotid tumor such as Warthin's tumor. The excision material was examined histopathologically. Immunohistochemical analysis showed that this carcinoma was positive for DOG1, SOX10, cytokeratin 7 and negative for mammaglobin. This salivary gland tumor was reported as a rare variant of ACC with lymphoid‐rich stroma. To improve the diagnostic accuracy, various morphological aspects of ACC should be considered in the pathological practice.