Carcinoid Tumors

被引:34
|
作者
Pasieka, Janice L. [1 ]
机构
[1] Univ Calgary, Div Surg Oncol & Gen Surg, Dept Surg, Calgary, AB T2N 2T0, Canada
关键词
Carcinoid; Neuroendocrine tumors; Treatment of prognosis; Review; NEUROENDOCRINE TUMORS; SURGICAL-TREATMENT; LIVER METASTASES; ENDOCRINE TUMORS; CHROMOGRANIN-A; MIDGUT; THERAPY; MANAGEMENT; SURGERY; CLASSIFICATION;
D O I
10.1016/j.suc.2009.06.008
中图分类号
R61 [外科手术学];
学科分类号
摘要
Carcinoid tumors, which arise from the enterochromaffin cells of the gastrointestinal tract, encompass a diverse group of neoplasms. Once thought to be "carcinoma-like," these neoplasms exhibit a biologic behavior that varies from an indolent, benign course to an aggressive, rapidly progressive, and deadly disease. Today the term carcinoid is reserved for neuroendocrine tumors arising from the small bowel or neuroendocrine tumors that can cause carcinoid syndrome. This newer terminology has yet to be universally adopted, adding to the confusion in the literature. For the general surgeon there are several "carcinoid" tumors that he or she must be familiar with because many of these lesions are encountered during emergency laparotomies or incidentally discovered during investigation for vague abdominal pain. This review focuses on the gastrointestinal neuroendocrine tumors that general surgeons are likely to encounter during their career.
引用
收藏
页码:1123 / +
页数:16
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