Vater壶腹神经内分泌肿瘤1例报告
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摘要
<正>1病例资料患者女性,67岁,因"间断性右上腹胀痛不适20 d"于2017年7月10日入院。既往体健。查体:上腹部深压痛。辅助检查:肝功能示AST 68. 9 U/L、ALT 71. 8 U/L,胆红素未提示升高,肿瘤标志物糖链抗原(CA) 19-9、CA125、神经元特异性烯醇化酶(neuron-specific enolase,NSE)在正常范围内。上腹部
引文
[1] Expert Committee on Neuroendocrine Tumors,Chinese Socie-ty of Clinical Oncology. Expert consensus on gastroenteropan-creatic neuroendocrine neoplasms in China(2016 Edition)[J]. Chin Clin Oncol,2016,21(10):927-946.(in Chi-nese)中国临床肿瘤学会神经内分泌肿瘤专家委员会.中国胃肠胰神经内分泌肿瘤专家共识(2016年版)[J].临床肿瘤学杂志,2016,21(10):927-946.
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[3] FRAENKEL M,KIM MK,FAGGIANO A,et al. Epidemiology ofgastroenteropancreatic neuroendocrine tumours[J]. BestPract Res Clin Gastroenterol,2012,26(6):691-703.
[4] MILANETTO AC,PASQUALI C,DA BROI M,et al. Ampullaryneuroendocrine neoplasms:Surgical experience of a rare andchallenging entity[J]. Langenbecks Arch Surg,2018,403(5):581-589.
[5] REESE WR,SHUJA A,NAEEM AN,et al. Su1666 clinical out-comes for neuroendocrine tumors of the duodenum and ampul-la of vater:A population-based study[J]. J GastrointestSurg,2014,18(2):354-362.
[6] YANG K,YUN SP,KIM S,et al. Clinicopathological featuresand surgical outcomes of neuroendocrine tumors of ampulla ofVater[J]. BMC Gastroenterol,2017,17(1):70.
[7] JUNG HN,MI HP,SEUNG KC,et al. MRI findings of an am-pulla of Vater neuroendocrine tumor with liver and lymph nodemetastasis:A case report[J]. Investig Magn Reson Imaging,2018,22(2):123-130.
[8] BAPTISTE GG,POSTLEWAIT LM,ETHUN CG,et al. Is therean optimal surgical approach to neuroendocrine tumors of theampulla? A single institution experience over 15 years[J]. AmSurg,2016,82(7):637-643.
[9] GAO WH,XIANG XX. Primary hepatic neuroendocrine neo-plasm:A report of 2 cases and literature review[J]. J ClinHepatol,2017,33(6):1149-1151.(in Chinese)高伟华,向晓星.原发性肝脏神经内分泌肿瘤2例报告并文献复习[J].临床肝胆病杂志,2017,33(6):1149-1151.
[10] RINDI G,ARNOLD R,FRED TB,et al. Nomenclature andclassification of neuroendocrine neoplasms of the digestivesystem[M]//WHO Classification of Tumours of the DigestiveSystem,4th ed. Lyon:IARC Press,2010:13-14.
[2] JULIE H,CALVIN HLL,MOISES C,et al. Exploring the risingincidence of neuroendocrine tumors:A population-based a-nalysis of epidemiology, metastatic presentation, and out-comes[J]. Cancer,2015,121(4):589-597.
[3] FRAENKEL M,KIM MK,FAGGIANO A,et al. Epidemiology ofgastroenteropancreatic neuroendocrine tumours[J]. BestPract Res Clin Gastroenterol,2012,26(6):691-703.
[4] MILANETTO AC,PASQUALI C,DA BROI M,et al. Ampullaryneuroendocrine neoplasms:Surgical experience of a rare andchallenging entity[J]. Langenbecks Arch Surg,2018,403(5):581-589.
[5] REESE WR,SHUJA A,NAEEM AN,et al. Su1666 clinical out-comes for neuroendocrine tumors of the duodenum and ampul-la of vater:A population-based study[J]. J GastrointestSurg,2014,18(2):354-362.
[6] YANG K,YUN SP,KIM S,et al. Clinicopathological featuresand surgical outcomes of neuroendocrine tumors of ampulla ofVater[J]. BMC Gastroenterol,2017,17(1):70.
[7] JUNG HN,MI HP,SEUNG KC,et al. MRI findings of an am-pulla of Vater neuroendocrine tumor with liver and lymph nodemetastasis:A case report[J]. Investig Magn Reson Imaging,2018,22(2):123-130.
[8] BAPTISTE GG,POSTLEWAIT LM,ETHUN CG,et al. Is therean optimal surgical approach to neuroendocrine tumors of theampulla? A single institution experience over 15 years[J]. AmSurg,2016,82(7):637-643.
[9] GAO WH,XIANG XX. Primary hepatic neuroendocrine neo-plasm:A report of 2 cases and literature review[J]. J ClinHepatol,2017,33(6):1149-1151.(in Chinese)高伟华,向晓星.原发性肝脏神经内分泌肿瘤2例报告并文献复习[J].临床肝胆病杂志,2017,33(6):1149-1151.
[10] RINDI G,ARNOLD R,FRED TB,et al. Nomenclature andclassification of neuroendocrine neoplasms of the digestivesystem[M]//WHO Classification of Tumours of the DigestiveSystem,4th ed. Lyon:IARC Press,2010:13-14.