Schlosnagle D C, Campbell W G
Cancer. 1981 Jun 1;47(11):2603-10. doi: 10.1002/1097-0142(19810601)47:11<2603::aid-cncr2820471115>3.0.co;2-z.
Two pancreatic tumors occurred in young women without detected functional symptoms. They had similar gross and histologic features and appeared to be of low grade malignancy. Case 1 was a typical example of the recently described entity referred to as papillary and solid neoplasm of the pancreas. Electron microscopic findings in this case indicated a duct cell origin, similar to previously reported cases. Case 2, also ultrastructurally similar, is unique in that it contained neurosecretory granules. Since considerable evidence indicated that cells of small pancreatic ducts give rise to islet cells, case 2 suggests that some tumors of ductal origin recapitulate the embryogenesis of the pancreatic islets and, therefore, may contain neurosecretory granules without showing the classic morphology of the more common pancreatic endocrine tumors.
两名年轻女性发生胰腺肿瘤,无功能性症状。它们具有相似的大体和组织学特征,看似低度恶性。病例1是最近描述的胰腺乳头状实性肿瘤典型病例。该病例的电镜检查结果显示为导管细胞起源,与先前报道的病例相似。病例2在超微结构上也相似,其独特之处在于含有神经分泌颗粒。由于大量证据表明胰腺小导管细胞可分化为胰岛细胞,病例2提示某些导管起源的肿瘤重现了胰岛的胚胎发育过程,因此可能含有神经分泌颗粒,而不表现出更常见胰腺内分泌肿瘤的典型形态。