摘要
神经内分泌肿瘤(neuroendocrine tumor,NET)在临床上较少见,多发生于支气管肺组织或消化道,发生在肝脏的NET多为胃肠胰神经内分泌肿瘤(gastrointestinal pancreatic neuroendocrine tumor,GEP-NET)转移而来。原发性肝脏神经内分泌肿瘤(primaryhepatic neuroendocrine tumor,PHNET)与转移性肝脏神经内分泌肿瘤(metastatic hepatic neuroendocrine tumor,MHNET)的鉴别缺乏特异性,原发性NET的诊断建立在排除继发性NET病变的基础上。现从分类、临床症状、血清学、影像学检查、鉴别诊断及治疗6个方面作一概述。
Neuroendocrine tumor (NET) is uncommon, mostly derived from the bronchial lung tissue or digestive tract, while occurred in the liver are mostly transfered from gastrointestinal pancreatic neuroendocrine tumors (GEP-NET). There are no specific differentiations of primary hepatic neuroendocrine tumor (PHNET) and metastatic hepatic neuroendocrine tumor (MHNET). The diagnosis of PHNET is based on the elimination of secondary NET disease. In this article, the classification, clinical symptoms, serology, imaging, differential diagnosis and treatment of the PHNET were reviewed.
作者
高伟华
向晓星
GAO Weihua;XIANG Xiaoxing(Subei People’s Hospital Affiliated to Clinical Medical College of Yangzhou University,Yangzhou 225001,China)
出处
《胃肠病学和肝病学杂志》
CAS
2019年第2期121-125,共5页
Chinese Journal of Gastroenterology and Hepatology
