The most common colorectal polyps found during routine colonoscopy were 270 adenomatous (52.4 %) cases. Of these, 155 (57.4 %) adenomatous polyps were high-risk category. Population prevalence data of colonic polyps in general population beyond the age of 50 years needs to be obtained.

Overview Mesenchymal tumors of the breast are rare. Few epithelial tumors also have mesenchymal components. It is crucial to identify these as per histogenesis. This can be facilitated by markers of epithelial–mesenchymal transition (EMT) Objectives The aim of this study was to categorize the breast lesions with mesenchymal morphology and to study EMT on immunohistochemistry (IHC). Materials and Methods This is a retrospective study of 5-year duration from January 2015 to December 2019. Inclusion criteria: all breast lesions showing mesenchymal/nonepithelial morphology, complete or partial, on histology. Exclusion criteria: Mammary carcinomas without any mesenchymal/nonepithelial morphology, fibroadenomas, and lymphomas. Demographics, clinical, gross examination, histology, and IHC findings of selected cases were reviewed and recorded. Three additional markers p53, E-cadherin, and β-catenin were performed. Statistical Analysis Used Frequency calculation for each variable (IHC). Results Thirteen (2.5%) out of total 510 breast specimens showed mesenchymal histology. Of these, five (38.5%) were metaplastic breast carcinomas (MBC), four (31%) were phyllodes tumor (PT), and one (7.7%) case each of malignant peripheral nerve sheath tumor, primary stromal sarcoma of breast, pseudoangiomatous stromal hyperplasia, and myofibroblastoma. Loss of E-cadherin was seen in 4/5 (80%) MBCs and was retained in ductal component of PTs. p53 was not expressed in any of the tumors except 3/5 (60%) MBCs. β-Catenin was aberrant in all MBCs. Conclusions Primary breast tumors with mesenchymal morphology present a spectrum ranging from benign mesenchymal, fibroepithelial neoplasms to malignant tumors of mesenchymal and epithelial origin. Loss of E-cadherin, expression of p53, and aberrant expression of β-catenin are suggestive of EMT and molecular heterogeneity of MBCs.

Introduction: Diagnosis of mucoepidermoid carcinoma (MEC) on fine-needle aspiration cytology (FNAC) is grim with important diagnostic pitfalls, leading to wrong treatment decisions. This study highlights uncommon mimics of MEC on FNAC smears of major salivary glands and compares the cytologic findings with definitive histopathology diagnosis for identification of potential diagnostic pitfalls. Methods: This is a retrospective descriptive study of MEC cases diagnosed over a duration of 5 years (April 2015–April 2020) at a tertiary care center with available preoperative FNAC and postoperative histopathology resection specimens. Results: Out of a total of 18 MEC cases diagnosed by histopathologic examination, 8 (44%) were wrongly diagnosed on preoperative FNAC as a different benign or malignant entity. Further details of these cases are shared in the text. Discussion: Although FNAC remains an important preoperative diagnostic tool in salivary gland lesions, utmost care is required in the cases of MEC which are notorious for misinterpretation on cytology. A number of uncommon mimics, both benign and malignant, need to be considered and carefully excluded to spare the patient of avoidable miseries of misdiagnosis. Conclusion: MECs of salivary glands can mimic the morphology of a variety of benign as well as malignant lesions on cytology with low cyto-histologic concordance especially in cystic lesions.