Unveiling lipid‐rich (“clear cell”) pancreatic neuroendocrine tumor: A small series of two cases with literature review

Abstract

AbstractThis study presents two cases of lipid‐rich pancreatic neuroendocrine tumors (PanNETs), a rare variant posing significant diagnostic challenges in fine needle aspiration (FNA) cytology and small biopsies. The first case involves an elderly male with a pancreatic tumor, displaying distinct cytoplasmic vacuoles, while the second case is a middle‐aged male present with a pancreatic tail mass exhibiting foamy cytoplasm and eccentric nuclei, infiltrating in the stroma. Both cases did not exhibit typical morphologic features of PanNET but demonstrated cytomorphologic features and infiltrative growth patterns that mimicked adenocarcinoma. Further work‐up demonstrated that both tumors were immunoreactive for synaptophysin and chromogranin, and were interpreted as well‐differentiated, PanNET, lipid‐rich variant. The study highlights the overlapping morphological features between lipid‐rich PanNETs and other pancreatic neoplasms and underscores the importance of comprehensive cytological and immunohistochemical analysis for accurately diagnosing this variant, particularly due to the risk of misinterpreting it as pancreatic adenocarcinoma. Recognizing lipid‐rich PanNETs is crucial for appropriate clinical management, as their identification can significantly impact treatment decisions and patient outcomes.