Kunz J, Amendt P, Buntrock P, Gottschalk J, Hahn von Dorsche H
Acta Histochem Suppl. 1986;33:233-41.
Fifteen endocrine pancreatic tumours (8 insulinomas, 3 gastrinomas, 1 vipoma, 3 tumours without hormonal activity) and two cases with dysplasia of the endocrine pancreas are reported. Immunohistochemical and electronmicroscopical investigations produced evidence of multihormonality in adenomas that clinically appeared to be monohormonal. The S-phase fraction of such tumours is below 1% which indicates their low proliferative potential. The malignancy of endocrine pancreatic tumours cannot be seen from cytochemical or histological symptoms; it can be established with certainty only from the presence of metastases. Multiple endocrine adenomas should suggest the possibility of hereditary endocrine polyadenomatosis. Hyperplasia and distribution disorder of the endocrine tissue as well as pathologically increased nesidioblastic activity represent the morphologic substrate of dysplasia of the endocrine pancreas as a potential cause of hyperinsulinaemic hypoglycaemia in infancy.
本文报告了15例内分泌性胰腺肿瘤(8例胰岛素瘤、3例胃泌素瘤、1例血管活性肠肽瘤、3例无激素活性的肿瘤)以及2例内分泌胰腺发育异常的病例。免疫组织化学和电子显微镜检查发现,临床上表现为单激素性的腺瘤存在多激素分泌现象。此类肿瘤的S期细胞比例低于1%,这表明其增殖潜能较低。内分泌性胰腺肿瘤的恶性程度无法通过细胞化学或组织学症状判断;只有发现转移才能确定其为恶性。多发性内分泌腺瘤应提示遗传性内分泌性多腺瘤病的可能性。内分泌组织的增生和分布紊乱以及病理上增加的胰岛母细胞活性是内分泌胰腺发育异常的形态学基础,而内分泌胰腺发育异常是婴儿期高胰岛素血症性低血糖的潜在原因。