Ooi A, Katsuda S, Nakanishi I, Kameya T, Yamaguchi K, Kitamura H, Hayakawa Y
Department of Surgery, Cancer Research Institute Hospital, Kanazawa University, Japan.
Ultrastruct Pathol. 1989 Jan-Feb;13(1):15-22. doi: 10.3109/01913128909051156.
We describe a case of pancreatic tumor in a 65-year-old woman with typical glucagonoma syndrome. Plasma glucagon (GL) and pancreatic polypeptide (PP) were markedly elevated up to 1404 and 1200 pg/ml, respectively. Histologic examination of the metastatic tumors in liver and lymph nodes showed endocrine-type tumors composed of GL-positive cells some of which coexpressed PP immunoreactivity. Electron microscopy revealed the tumor cells with single-type secretory granules similar to normal A cell granules. Double immunogold staining demonstrated both GL and PP immunoreactivities in the same secretory granules. Biologic and diagnostic significance of coexpression of PP and GL in a single secretory granules of pancreatic endocrine tumors is discussed briefly.