| Literature DB >> 16804989 |
Jaques Waisberg1, Leandro Luongo de Matos, Ana Maria do Amaral Antonio Mader, Sergio Pezzolo, Esmeralda Miristene Eher, Vera Luiza Capelozzi, Manlio Basilio Speranzini.
Abstract
Poorly differentiated gastric neuroendocrine carcinomas, although rare, deserve particular attention, as they are aggressive and have an extremely poor prognosis. In this report we describe a gastric neuroendocrine carcinoma with rapidly fatal outcome. Immunohistological staining of the resected specimens revealed that the tumor was an endocrine carcinoma. The tumor disclosed intense immunoreactivity to pan-neuroendocrine markers and diffuse somatostatin immunoreactivity. There were no psammoma bodies and no demonstrable association with von Recklinghausen's neurofibromatosis. In the gastrointestinal tract, neuroendocrine tumors producing predominantly somatostatin have been described only in the duodenum. To the best of our knowledge, the present report is the second case report of a neuroendocrine gastric carcinoma expressing diffusely somatostatin as the only neuroendocrine regulatory peptide.Entities:
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Year: 2006 PMID: 16804989 PMCID: PMC4087952 DOI: 10.3748/wjg.v12.i24.3944
Source DB: PubMed Journal: World J Gastroenterol ISSN: 1007-9327 Impact factor: 5.742