Copyright
©The Author(s) 2019.
World J Clin Cases. Sep 6, 2019; 7(17): 2413-2419
Published online Sep 6, 2019. doi: 10.12998/wjcc.v7.i17.2413
Published online Sep 6, 2019. doi: 10.12998/wjcc.v7.i17.2413
Figure 2 Tumors usually exhibit nil mitotic activity and a low Ki67 proliferation index of less than 3%, compatible with well differentiated neuroendocrine tumors, grade 1.
A: A nodule of neuroendocrine tumor nest of cells with nuclei showing “salt and pepper” chromatin with negligible mitotic activity and absent necrosis (HE, 400×); B: Ki67 proliferation index of 5%, consistent with a well differentiated neuroendocrine tumor G2 (Ki67 immunostain, 400×); C: Nest of tumors cells, arranged in nodules, showing intermediate grade cytological atypia characterized by abundant amphophilic cytoplasm, enlarged nuclei with open chromatin and nucleoli; D: Ki67 proliferation index of more than 20%, consistent with a well differentiated neuroendocrine tumor G3 (Ki67 immunostain, 400×).
- Citation: Algashaamy K, Garcia-Buitrago M. Multifocal G1-G2 gastric neuroendocrine tumors: Differentiating between Type I, II and III, a clinicopathologic review. World J Clin Cases 2019; 7(17): 2413-2419
- URL: https://www.wjgnet.com/2307-8960/full/v7/i17/2413.htm
- DOI: https://dx.doi.org/10.12998/wjcc.v7.i17.2413