Sun Ke-Kang, Liu Gang, Shen Xiaojun, Wu Xiaoyang
Department of Gastrointestinal Surgery, Kunshan First People's Hospital Affiliated to Jiangsu University, Kunshan, Jiangsu 215300, P.R. China.
Oncol Lett. 2016 Aug;12(2):1602-1604. doi: 10.3892/ol.2016.4753. Epub 2016 Jun 17.
Small bowel adenocarcinoma is part of the tumor spectrum of Lynch syndrome, which is caused by germline mutations in the mismatch repair genes. The present study describes the case of a 51-year-old man fulfilling the Amsterdam II criteria for Lynch syndrome, who had a 15-mm early-stage colorectal cancer resected endoscopically from the ascending colon. Due to upper abdominal discomfort after eating and consequent anorexia, a computed tomography scan performed 1 month later showed a tumoral mass of the upper jejunum with local lymphadenopathy. The laparotomy revealed a completely obstructing mass. Intraoperative frozen section showed a small bowel adenocarcinoma. Subsequent genetic testing confirmed the germline mutation of mutL homolog 1. The patient received 6 cycles of an adjuvant folinic acid, fluorouracil and ocaliplatin chemotherapy regimen. The latest CT scan, 16 months after the chemotherapy, did not show any recurrence. This case highlights the importance of considering the possibility of small bowel adenocarcinoma in patients with upper bowel obstruction, particularly for patients with Lynch syndrome.
小肠腺癌是林奇综合征肿瘤谱的一部分,林奇综合征由错配修复基因的种系突变引起。本研究描述了一例符合林奇综合征阿姆斯特丹II标准的51岁男性病例,该患者经内镜切除了升结肠处一个15毫米的早期结直肠癌。由于进食后上腹部不适及随之而来的厌食,1个月后进行的计算机断层扫描显示空肠上段有一个肿瘤性肿块,并伴有局部淋巴结病。剖腹探查发现一个完全阻塞性肿块。术中冰冻切片显示为小肠腺癌。随后的基因检测证实了mutL同源物1的种系突变。该患者接受了6个周期的亚叶酸、氟尿嘧啶和奥沙利铂辅助化疗方案。化疗16个月后的最新CT扫描未显示任何复发迹象。该病例突出了对于上肠梗阻患者,尤其是林奇综合征患者,考虑小肠腺癌可能性的重要性。