| Literature DB >> 2537546 |
A Ooi1, S Katsuda, I Nakanishi, T Kameya, K Yamaguchi, H Kitamura, Y Hayakawa.
Abstract
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.Entities:
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Year: 1989 PMID: 2537546 DOI: 10.3109/01913128909051156
Source DB: PubMed Journal: Ultrastruct Pathol ISSN: 0191-3123 Impact factor: 1.094