Li Tian-Nv, Liu Zijun, Zhang Yingdong, Wang Feng
Nuclear Medicine, The First Affiliated Hospital of Nanjing Medical Univerity, Nanjing, Jiangsu, China.
Department of General Surgery, Nanjing First Hospital, Nanjing Medical University, Nanjing, China.
BMJ Case Rep. 2018 Jun 29;2018:bcr-2018-224281. doi: 10.1136/bcr-2018-224281.
We describe a middle-aged woman with recurrent hypoglycaemia, who confirmed with rectum G1 neuroendocrine tumour (NET) 6 years ago. Biochemical assay showed high concentration of serum insulin and C-peptide associated with hypoglycaemia. Because of recurrent hypoglycaemia in June 2015, she underwent a resection of the tail of the pancreas. However, hypoglycaemia attack happened more frequently and severely. Ga-DOTA-NOC positron emission tomography/CT revealed five foci in the pelvis with intense uptake. Immediately after excision of the pelvic lesions, insulin and C-peptide decreased to normal levels promptly, and therefore, serum glucose increased significantly. Hypoglycaemia was disappeared, and insulin and C-peptide were normal at 2 years follow-up after surgery. Immunohistochemistry validated the primary rectum NET and pelvic tumours expressed with higher insulin, somatostatin receptor and glucagon-like peptide-1. This is the first reported ectopic pelvic insulinomas secondary to rectum NET, which may originate both from neuroendocrine cells in the rectum and pelvic tissues.
我们描述了一位患有复发性低血糖症的中年女性,她在6年前被确诊为直肠G1神经内分泌肿瘤(NET)。生化检测显示血清胰岛素和C肽浓度升高并伴有低血糖症。由于2015年6月出现复发性低血糖症,她接受了胰腺尾部切除术。然而,低血糖发作变得更加频繁和严重。Ga-DOTA-NOC正电子发射断层扫描/计算机断层扫描(PET/CT)显示盆腔有五个摄取强烈的病灶。切除盆腔病变后,胰岛素和C肽立即迅速降至正常水平,因此血糖显著升高。低血糖症消失,术后2年随访时胰岛素和C肽正常。免疫组织化学证实原发性直肠NET和盆腔肿瘤表达较高的胰岛素、生长抑素受体和胰高血糖素样肽-1。这是首例报道的继发于直肠NET的异位盆腔胰岛素瘤,其可能起源于直肠和盆腔组织中的神经内分泌细胞。