[Mixed adenoneuroendocrine carcinoma: case report].

Ángel A Hernández-Moreno, Carlos E Durón-Gutiérrez, Sheyla P Serrano-González, Grettel León-Martínez, José G Arroyo-Del-Castillo
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引用次数: 0

Abstract

Introducción: Mixed adenoneuroendocrine carcinoma is a rare tumor of the gastrointestinal tract with double differentiation into adenomatous and neuroendocrine carcinoma, each component with at least 30%.

Case report: A 60-year-old female with acute abdominal pain. Surgical treatment was decided, finding a tumor at the level of the cecum and ascending colon, a right hemicolectomy and ileostomy were performed.

Discussion: Mixed adenoneuroendocrine carcinoma can appear in various organs. They are highly malignant tumors, with a high risk of metastasis.

Conclusions: These tumors do not present symptoms or specific radiological or laboratory findings; diagnosis depends on postoperative histopathological and immunohistochemical studies.

[混合性腺内分泌癌:病例报告]
介绍:腺神经内分泌混合癌是一种罕见的胃肠道肿瘤,具有腺瘤样癌和神经内分泌癌双重分化,每种成分至少占30%:病例报告:一名 60 岁女性,急性腹痛。决定进行手术治疗,发现肿瘤位于盲肠和升结肠水平,于是进行了右半结肠切除术和回肠造口术:讨论:混合型腺内分泌癌可出现在多个器官。讨论:混合腺神经内分泌癌可出现在多个器官,是高度恶性肿瘤,转移风险高:这些肿瘤没有症状,也没有特殊的放射学或实验室检查结果;诊断取决于术后组织病理学和免疫组化检查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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