Kunz J, Amendt P, Hahn von Dorsche H, Gerl H, Knappe E, Lorenz D
Zentralbl Allg Pathol. 1983;127(5-6):375-83.
The changes of the endocrine pancreas in two cases of pluriglandular neoplasia type I were studied. A 15 year-old girl showed an amyloid containing ductuloinsular B cell adenoma, microadenomas and nesidioblastic processes. The simultaneous presence of hyperprolactinemia and nephrolithiasis indicates the existence of the endocrine polyadenomatosis. A 33 year-old woman had four amyloid containing B cell adenomas with ductular proliferation, a main cell adenoma of the parathyroid and a prolactinoma of the adenohypophysis. Solitary or multiple ductuloinsular adenomas, amyloid of the endocrine type and nesidioblastic activity are not specific features of the endocrine pancreas in pluriglandular adenomatosis. Similar structures can be found in isolated islet cell tumors or in nesidioblastosis. Ductuloinsular proliferations can also be observed in chronic pancreatitis.
对两例Ⅰ型多腺体肿瘤患者的内分泌胰腺变化进行了研究。一名15岁女孩表现为含有淀粉样物质的导管胰岛B细胞腺瘤、微腺瘤和胰岛母细胞增生。高催乳素血症和肾结石同时存在提示内分泌性多腺瘤病的存在。一名33岁女性有四个含有淀粉样物质的B细胞腺瘤伴导管增生、甲状旁腺主细胞腺瘤和腺垂体催乳素瘤。孤立或多发的导管胰岛腺瘤、内分泌型淀粉样物质和胰岛母细胞活性并非多腺体腺瘤病中内分泌胰腺的特异性特征。类似结构可见于孤立性胰岛细胞瘤或胰岛母细胞增生症。慢性胰腺炎中也可观察到导管胰岛增生。