Department of Pathology, Beth Israel Deaconess Medical Center, 330 Brookline Avenue, Boston, MA 02215, USA; Harvard Medical School, Boston, MA, USA.
Surg Pathol Clin. 2020 Sep;13(3):377-397. doi: 10.1016/j.path.2020.04.002.
The latest WHO classification cleanly divides gastrointestinal neuroendocrine neoplasms into neuroendocrine tumor (NET; well-differentiated, any grade) and neuroendocrine carcinoma (NEC; poorly differentiated, high-grade by definition), along with mixed neuroendocrine-non-neuroendocrine neoplasms. NECs are always aggressive, with multiple mutations; they are treated with chemotherapy. NETs have widely different presentations, behavior, and management depending on site of origin. Esophageal examples are vanishingly rare. Most gastric and appendiceal tumors are indolent, as are many colonic and rectal tumors. The duodenum is home to some unusual variants of NET, and jejunal/ileal NETs frequently metastasize, which impacts their staging and clinical management.
世界卫生组织(WHO)最新分类法将胃肠道神经内分泌肿瘤明确分为神经内分泌肿瘤(NET;分化良好,任何级别)和神经内分泌癌(NEC;分化差,定义为高级别),并包含混合性神经内分泌-非神经内分泌肿瘤。NEC 通常具有侵袭性,存在多种突变,采用化疗治疗。NET 的表现、行为和治疗因起源部位而异,差异极大。食管部位的 NET 极为罕见。大多数胃和阑尾肿瘤生长缓慢,同样,很多结肠和直肠肿瘤也是如此。十二指肠是一些不常见 NET 变异型的发源地,空肠/回肠 NET 常发生转移,这影响其分期和临床管理。