Naito Shigetoshi, Naito Masayasu, Yamamoto Nobuharu, Kume Tohru, Hosino Seiichirou, Kinjyo Yoshinao, Naito Yoshiki, Naito Hisanori, Hasegawa Suguru
Department of Gastroenterological Surgery, Faculty of Medicine, Fukuoka University, Jonan-ku, Fukuoka 814-0180, Japan.
Naito Hospital, Kurume, Fukuoka 830-0038, Japan.
Mol Clin Oncol. 2020 Mar;12(3):225-229. doi: 10.3892/mco.2019.1971. Epub 2019 Dec 24.
Gallbladder neuroendocrine tumors (GB-NETs) comprise only 0.5% of all NET cases, and their biology has been incompletely characterized. In the present study we report the case of a 50-year-old male patient with GB-NET who was admitted to Naito Hospital with diarrhea as the main complaint. At initial diagnosis, serum carcinoembryonic antigen (CEA) and carbohydrate antigen 19-9 (CA19-9) levels were within the normal range. Abdominal ultrasonography and contrast-enhanced computed tomography (CT) revealed gallbladder adenomyomatosis and cholecystitis, and an 8-mm pedunculated polypoid lesion was found in the neck of the gallbladder using drip infusion cholecystocholangiography-CT. As it was considered a benign polyp, laparoscopic cholecystectomy was performed. Pathological examination revealed a polypoid lesion that comprised NET cells with a cord-like or ribbon-like arrangement, and the cells exhibited positive immunostaining for chromogranin A and synaptophysin. In addition, immunohistochemical staining showed a Ki-67 index (i.e., proliferation index) of <1%, and no necrosis or mitotic figures were observed in the background. Based on these observations, we diagnosed the following: GB-NET, G1, 10x12 mm in size and located in the gallbladder neck. According to the World Health Organization 2010 classification, NET G1 is a well-differentiated tumor, with the tumor cells having a low proliferative potential [Ki-67 index ≤2%; mitotic figure number <2 (/10 HPF)]. It is regarded as a low- to mild-grade malignancy. Low-grade GB-NET occurs relatively rarely, and no clear guidelines have been formulated regarding its surgical treatment, such as minimal surgical excision margins or lymph node dissection. Detailed treatment recommendations should be developed after systematic studies of additional cases of GB-NET.
胆囊神经内分泌肿瘤(GB-NETs)仅占所有神经内分泌肿瘤病例的0.5%,其生物学特性尚未完全明确。在本研究中,我们报告了一例以腹泻为主诉入院的50岁男性GB-NET患者。初诊时,血清癌胚抗原(CEA)和糖类抗原19-9(CA19-9)水平在正常范围内。腹部超声和增强计算机断层扫描(CT)显示胆囊腺肌症和胆囊炎,通过滴注式胆囊胆管造影CT在胆囊颈部发现一个8毫米的带蒂息肉样病变。由于考虑为良性息肉,遂行腹腔镜胆囊切除术。病理检查显示息肉样病变由呈条索状或带状排列的神经内分泌肿瘤细胞组成,这些细胞嗜铬粒蛋白A和突触素免疫染色呈阳性。此外,免疫组化染色显示Ki-67指数(即增殖指数)<1%,背景中未观察到坏死或核分裂象。基于这些观察结果,我们诊断如下:GB-NET,G1级,大小为10×12毫米,位于胆囊颈部。根据世界卫生组织2010年分类,NET G1是一种高分化肿瘤,肿瘤细胞增殖潜能低[Ki-67指数≤2%;核分裂象数<2(/10 HPF)]。它被视为低至中度恶性肿瘤。低度GB-NET相对少见,关于其手术治疗,如最小手术切缘或淋巴结清扫,尚未制定明确的指南。应在对更多GB-NET病例进行系统研究后制定详细的治疗建议。