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[儿童胰腺成神经细胞瘤中嗜铬粒蛋白A的免疫组织化学检测及形态学结果]

[Immunohistochemical detection of chromogranin A and morphometric findings in pancreatic nesidioblastosis in children].

作者信息

Kunz J, Haberland H, Schmidt A, Amendt P

机构信息

Institut für Pathologie des Bezirkskrankenhauses Potsdam, Deutschland.

出版信息

Acta Histochem. 1990;89(2):131-40.

PMID:2093263
Abstract

The histologic features and morphometric data of the endocrine pancreas (surgical specimens) of 12 infants suffering from persistent hyperinsulinemic hypoglycemia are reported. In 3 cases, a focal nesidioblastosis, in another 3 cases, a diffuse nesidioblastosis were observed. 2 infants demonstrate B-cell adenomata and 4 adenomata combined with a diffuse nesidioblastosis. In respect to volume density of the endocrine pancreas and diameter of the islets, there are no differences between cases with diffuse nesidioblastosis and age-matched controls. Structural changes of the endocrine pancreas in cases with nesidioblastosis are detectable by their chromogranin-A-immunoreactivity. Further investigations are necessary to clarify if there are disturbances in the relationships between chromogranin A and peptide hormones additionally to structural changes in the pancreas.

摘要

报告了12例持续性高胰岛素血症低血糖症婴儿内分泌胰腺(手术标本)的组织学特征和形态计量学数据。3例观察到局灶性胰岛细胞增殖症,另外3例观察到弥漫性胰岛细胞增殖症。2例婴儿表现为B细胞腺瘤,4例为腺瘤合并弥漫性胰岛细胞增殖症。就内分泌胰腺的体积密度和胰岛直径而言,弥漫性胰岛细胞增殖症病例与年龄匹配的对照组之间没有差异。胰岛细胞增殖症病例中内分泌胰腺的结构变化可通过嗜铬粒蛋白A免疫反应性检测到。需要进一步研究以阐明除胰腺结构变化外,嗜铬粒蛋白A与肽类激素之间的关系是否存在紊乱。

相似文献

1
[Immunohistochemical detection of chromogranin A and morphometric findings in pancreatic nesidioblastosis in children].[儿童胰腺成神经细胞瘤中嗜铬粒蛋白A的免疫组织化学检测及形态学结果]
Acta Histochem. 1990;89(2):131-40.
2
Diffuse and focal nesidioblastosis. A clinicopathological study of 24 patients with persistent neonatal hyperinsulinemic hypoglycemia.弥漫性和局灶性胰岛细胞增殖症。24例持续性新生儿高胰岛素血症性低血糖症患者的临床病理研究。
Am J Surg Pathol. 1989 Sep;13(9):766-75.
3
Pancreatic B-cell proliferation in persistent hyperinsulinemic hypoglycemia of infancy: an immunohistochemical study of 18 cases.婴儿持续性高胰岛素血症性低血糖症中胰腺β细胞增殖:18例免疫组织化学研究
Mod Pathol. 1998 May;11(5):444-9.
4
Production of pro-insulin, C-peptide, and insulin in nesidioblastosis, focal islet-cell adenomatosis, and genuine insulomas. A correlated radioimmunochemical, immunohistochemical, and ultrastructural investigation with particular regard to the occurrence of argyrophil and pro-insulin immunoreactive cells.胰岛母细胞增生症、局灶性胰岛细胞瘤和真性胰岛素瘤中胰岛素原、C肽和胰岛素的产生。一项相关的放射免疫化学、免疫组织化学和超微结构研究,特别关注嗜银细胞和胰岛素原免疫反应性细胞的出现情况。
Diabetes Res. 1988 Aug;8(4):151-63.
5
Disorders of the endocrine pancreas.胰腺内分泌紊乱。
Prog Pediatr Surg. 1983;16:51-61.
6
Case report: focal nesidioblastosis ("nesidioblastoma") in an adult.病例报告:成人局灶性胰岛细胞瘤(“胰岛细胞瘤”)。
Hum Pathol. 2010 Mar;41(3):447-51. doi: 10.1016/j.humpath.2009.09.002. Epub 2009 Dec 11.
7
Adult nesidiodysplasia.成人胰岛细胞增殖症
Semin Diagn Pathol. 1984 Feb;1(1):43-53.
8
Surgical management of islet cell dysmaturation syndrome in young children.幼儿胰岛细胞发育异常综合征的外科治疗
Surg Gynecol Obstet. 1990 Oct;171(4):321-5.
9
Diffuse nesidioblastosis as a cause of hyperinsulinemic hypoglycemia in adults: a diagnostic and therapeutic challenge.成人弥漫性胰岛细胞增殖症作为高胰岛素血症性低血糖的病因:诊断与治疗挑战
Surgery. 2007 Feb;141(2):179-84; discussion 185-6. doi: 10.1016/j.surg.2006.04.015.
10
Immunohistochemical, morphometric, and clinical studies of the pancreatic islets in infants with persistent neonatal hypoglycemia of familial type with hyperinsulinism and nesidioblastosis.
Acta Biol Med Ger. 1981;40(1):39-54.

引用本文的文献

1
A new multilabeling technique for simultaneous demonstration of different islet cells in permanent slides.一种用于在永久性载玻片上同时显示不同胰岛细胞的新型多重标记技术。
Int J Pancreatol. 1993 Apr;13(2):139-42. doi: 10.1007/BF02786082.