[混合性腺神经内分泌癌：病例报告]
[Mixed adenoneuroendocrine carcinoma: case report].
作者信息
Hernández-Moreno Ángel A, Durón-Gutiérrez Carlos E, Serrano-González Sheyla P, León-Martínez Grettel, Arroyo-Del-Castillo José G
机构信息
Servicio de Cirugía Plástica y Reconstructiva, Hospital Regional Lic. Adolfo López Mateos, Instituto de Seguridad y Servicios Sociales de los Trabajadores del Estado (ISSSTE), Ciudad de México, México.
Servicio de Cirugía General, Hospital General Tacuba, ISSSTE, Ciudad de México, México.
出版信息
Cir Cir. 2024 Feb 12;92(5):674-678. doi: 10.24875/CIRU.21000713.
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.
引言
混合性腺神经内分泌癌是一种罕见的胃肠道肿瘤，具有腺管和神经内分泌癌的双重分化，每种成分至少占30%。
病例报告
一名60岁女性，伴有急性腹痛。决定进行手术治疗，在盲肠和升结肠水平发现一个肿瘤，实施了右半结肠切除术和回肠造口术。
讨论
混合性腺神经内分泌癌可出现在多个器官。它们是高度恶性肿瘤，转移风险高。
结论
这些肿瘤没有症状或特异性的影像学或实验室检查结果；诊断依赖于术后组织病理学和免疫组化研究。
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