Secretory carcinoma of salivary glands at the National Cancer Institute: A 20-year retrospective clinical, pathological, immunohistochemical and molecular study

• Published in: Oral oncology 2021-06, Vol.117, p.105198-105198, Article 105198
• Main Authors: Alves, Lísia Daltro Borges, de Melo, Andreia Cristina, de Lima Araujo, Luiz Henrique, Thiago, Leandro Souza, dos Santos Guimarães, Isabella, Fernandes, Priscila Valverde, Rodrigues, Elizangela Marques, Dias, Fernando Luiz, Antunes, Héliton Spindola, Eisenberg, Ana Lucia Amaral, Cohen Goldemberg, Daniel
• Format: Article
• Language: English
• Subjects: Acinic cell carcinoma; Biomarkers, Tumor - genetics; Biomarkers, Tumor - metabolism; Carcinoma, Acinar Cell - metabolism; Carcinoma, Acinar Cell - pathology; Cross-Sectional Studies; Droplet digital PCR; ETV6-NTRK3; Humans; Mammary analog secretory carcinoma; National Cancer Institute (U.S.); Retrospective Studies; Salivary gland neoplasms; Salivary Gland Neoplasms - metabolism; Salivary Gland Neoplasms - pathology; United States
• ISSN: 1368-8375; 1879-0593
• DOI: 10.1016/j.oraloncology.2021.105198

This study aim was to review cases of acinic cell carcinoma (the main differential diagnosis of secretory carcinoma) that were diagnosed and treated at the National Cancer Institute of Brazil (INCA) between 1996 and 2016. The primary objective was to identify underdiagnosed cases of secretory carcinoma via a clinical, immunopathological and molecular reassessment. This is a cross sectional study, with retrospective data collection from medical records and histological specimen review, with staining for periodic acid-Schiff (PAS) and PAS with diastase, immunohistochemistry for S-100, mammaglobin, and DOG-1, and droplet digital RT-PCR for ETV6-NTRK3. The Research Ethics Committee approved this study, and the patients allowed their participation through informed consent. Eighty-three cases of acinic cell carcinoma were diagnosed and treated in the specified period at INCA, of which, seven had their diagnosis changed to secretory carcinoma. The present study adds seven cases of secretory carcinoma to the literature, contributing to a better understanding of the epidemiological, histological, immunohistochemical and molecular characteristics of this recently described tumor. Also, the use of a comprehensive diagnostic approach, including immunohistochemical and molecular methods, along with classical morphological studies, allowed the reclassification of acinic cell carcinoma to secretory carcinoma.