Waisberg Jaques, de Matos Leandro Luongo, do Amaral Antonio Mader Ana Maria, Pezzolo Sergio, Eher Esmeralda Miristene, Capelozzi Vera Luiza, Speranzini Manlio Basilio
Department of Surgery, Faculty of Medicine of ABC, Santo André, Braz.
World J Gastroenterol. 2006 Jun 28;12(24):3944-7. doi: 10.3748/wjg.v12.i24.3944.
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.
低分化胃神经内分泌癌虽然罕见,但因其具有侵袭性且预后极差,值得特别关注。在本报告中,我们描述了一例具有快速致命结局的胃神经内分泌癌。对切除标本进行免疫组织化学染色显示,该肿瘤为内分泌癌。肿瘤对泛神经内分泌标志物显示出强烈的免疫反应性,且弥漫性生长抑素免疫反应阳性。未见砂粒体,也未发现与冯雷克林霍增氏神经纤维瘤病有明显关联。在胃肠道中,主要产生生长抑素的神经内分泌肿瘤仅在十二指肠中有过描述。据我们所知,本报告是第二例关于弥漫性表达生长抑素作为唯一神经内分泌调节肽的胃神经内分泌癌的病例报告。