Maisani J E, Turbellier J M, Krys H, Brassier D
J Chir (Paris). 1985 Jun-Jul;122(6-7):383-6.
Non-secreting tumors of pancreatic islets of Langerhans are now rarely encountered as a result of the increasing performance of techniques for detecting the different hormones of insular origin or their precursors. Histologically, these tumors, that can be termed nesidioblastomas of the pancreas, have a poorly defined potential course, but there is a definite risk of malignancy. A case is reported of a pancreatic nesidioblastoma located in two regions, treatment being by total duodenopancreatectomy with a good result at 4-year follow up review. A bibliographic list of 13 published reports in the international literature is provided.
由于检测胰岛源性不同激素或其前体的技术应用日益广泛,目前朗格汉斯胰岛非分泌性肿瘤已较少见。从组织学上看,这些肿瘤可称为胰腺成胰岛细胞瘤,其发展过程尚不明确,但存在恶变的明确风险。本文报告一例位于两个部位的胰腺成胰岛细胞瘤病例,通过十二指肠胰腺全切术进行治疗,4年随访结果良好。文中还提供了国际文献中13篇已发表报告的书目清单。