Mixed adenoneuroendocrine carcinoma: case report

被引:0
|
作者
Hernandez-Moreno, Angel A. [1 ]
Duron-Gutierrez, Carlos E. [2 ]
Serrano-Gonzalez, Sheyla P. [2 ]
Leon-Martinez, Grettel [3 ]
Arroyo-Del-Castillo, Jose G. [4 ]
机构
[1] Hosp Reg Lic Adolfo Lopez Mateos, Serv Cirugia Plast & Reconstruct, Inst Seguridad & Serv Sociales Trabajadores Estad, Mexico City, DF, Mexico
[2] Hosp Gen Tacuba, Serv Cirugia Gen, ISSSTE, Mexico City, DF, Mexico
[3] Hosp Gen Tacuba, Serv Anat Patol, ISSSTE, Mexico City, DF, Mexico
[4] Secretaria Salud Ciudad Mexico, Inst Nacl Neurol & Neurocirugia, Serv Neurocirugia, Mexico City, DF, Mexico
来源
CIRUGIA Y CIRUJANOS | 2024年 / 92卷 / 05期
关键词
Mixed adenoneuroendocrine carcinoma; Adenocarcinomatous differentiation; Neuroendocrine differentiation; Colorectal cancer;
D O I
10.24875/CIRU.21000713
中图分类号
R61 [外科手术学];
学科分类号
摘要
Introducci & oacute;n: 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.
引用
收藏
页码:674 / 678
页数:5
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