Anzai Hiroyuki, Kazama Shinsuke, Kiyomatsu Tomomichi, Nishikawa Takeshi, Tanaka Toshiaki, Tanaka Junichiro, Hata Keisuke, Kawai Kazushige, Yamaguchi Hironori, Nozawa Hiroaki, Kanazawa Takamitsu, Ushiku Tetsuo, Ishihara Soichiro, Sunami Eiji, Fukayama Masashi, Watanabe Toshiaki
Division of Surgical Oncology, Department of Surgery, Faculty of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8655, Japan.
Department of Pathology, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8655, Japan.
World J Surg Oncol. 2015 May 12;13:180. doi: 10.1186/s12957-015-0590-x.
Alpha-fetoprotein (AFP)-producing rectal cancer is very rare, and this type of cancer frequently metastasizes to the liver with a poor prognosis. To date, only 11 cases of AFP-producing colorectal cancer have been reported.
A 41-year-old woman was first presented to the hospital for anal bleeding. An elevated tumor with a central shallow depression in the lower rectum was detected by colonoscopy. Transanal excision was performed, and the histology revealed adenocarcinoma. Further immunohistopathological examination revealed that the tumor was an AFP-producing adenocarcinoma of the rectum. Although local resection was performed 2 months before the diagnosis of AFP tumor, the serum AFP level was normal. The depth of the submucosal invasion was 5,000 μm, and there was venous invasion. Also, no lymphatic invasion was detected. Therefore, additional surgical resection with lymph node dissection was conducted, and the patient underwent laparoscopic intersphincteric resection. No residual cancer was identified in the surgical specimens, and there was no evidence of lymph node metastasis. The patient was discharged 18 days postoperatively, and 12 months after the operation, there are no signs of recurrence.
To the best of our knowledge, this is the first case of an AFP-producing rectal cancer that was diagnosed at an early stage.
产生甲胎蛋白(AFP)的直肠癌非常罕见,这类癌症常转移至肝脏,预后较差。迄今为止,仅报道过11例产生AFP的结直肠癌病例。
一名41岁女性因肛门出血首次入院。结肠镜检查发现直肠下段有一个中央浅凹陷的隆起性肿物。行经肛门切除术,组织学检查显示为腺癌。进一步的免疫组织病理学检查显示该肿瘤为直肠产生AFP的腺癌。尽管在诊断AFP肿瘤前2个月已进行局部切除,但血清AFP水平正常。黏膜下浸润深度为5000μm,存在静脉侵犯。此外,未检测到淋巴侵犯。因此,进行了额外的手术切除及淋巴结清扫,患者接受了腹腔镜括约肌间切除术。手术标本中未发现残留癌,也没有淋巴结转移的证据。患者术后18天出院,术后12个月无复发迹象。
据我们所知,这是首例早期诊断的产生AFP的直肠癌病例。