BPG is committed to discovery and dissemination of knowledge
Editorial
Copyright ©The Author(s) 2025.
World J Gastrointest Oncol. Oct 15, 2025; 17(10): 110570
Published online Oct 15, 2025. doi: 10.4251/wjgo.v17.i10.110570
Figure 1
Figure 1 Photomicrographs of well-differentiated pancreatic ductal adenocarcinoma. A: Low power view of fine needle biopsy that was obtained using endoscopic ultrasound. The glass slide showed > 2000 pancreatic ductal adenocarcinoma tumor cells which is very helpful for ancillary studies (original magnification × 20); B: Higher power view of one of the cores from Figure 1A showing a well-differentiated pancreatic ductal adenocarcinoma (the well-differentiated glands can be seen on the left and an islet of Langerhans on the right) (original magnification × 100).
Figure 2
Figure 2 Photomicrographs of poorly-differentiated pancreatic ductal adenocarcinoma. A: Section from a pancreaticoduodenectomy specimen showing poorly differentiated pancreatic ductal adenocarcinoma of the pancreatic head. There are poorly formed infiltrative glands in a desmoplastic stroma (original magnification × 100); B: Ki67 immunohistochemistry slide from same case. The positive tumor cell nuclei are brown whereas the negative are blue. The Ki67 Labelling index in this field is 9.4%. Most studies for pancreatic ductal adenocarcinoma use the average count, but for pancreatic neuroendocrine neoplasms, the guidelines mandate selecting the hotspots.