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首页> 外文期刊>World Journal of Gastroenterology >Hyperinsulinemic hypoglycemia due to adult nesidioblastosis in insulin-dependent diabetes.
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Hyperinsulinemic hypoglycemia due to adult nesidioblastosis in insulin-dependent diabetes.

机译:在胰岛素依赖型糖尿病中,成年的成神经细胞成纤维细胞病引起的高胰岛素低血糖。

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摘要

In neonates, persistent hyperinsulinemic hypoglycemia (PHH) is associated with nesidioblastosis. In adults, PHH is usually caused by solitary benign insulinomas. We report on an adult patient who suffered from insulin-dependent diabetes mellitus, and subsequently developed PHH caused by diffuse nesidioblastosis. Mutations of the MEN1 and Mody (2/3) genes were ruled out. Preoperative diagnostic procedures, the histopathological criteria and the surgical treatment options of adult nesidioblastosis are discussed. So far only one similar case of adult nesidioblastosis subsequent to diabetes mellitus II has been reported in the literature. In case of conversion of diabetes into hyperinsulinemic hypoglycemia syndrome, nesidioblastosis in addition to insulinoma should be considered.
机译:在新生儿中,持续性高胰岛素血症性低血糖症(PHH)与成纤维细胞病有关。在成人中,PHH通常是由孤立的良性胰岛素瘤引起的。我们报道了一名患有胰岛素依赖型糖尿病并随后因弥漫性奈瑟氏成纤维细胞病而引起的PHH的成年患者。排除了MEN1和Mody(2/3)基因的突变。讨论了成人奈瑟成纤维细胞病的术前诊断程序,组织病理学标准和外科治疗方案。迄今为止,文献中仅报道了另一例类似的继发于II型糖尿病的成人成纤维细胞病。如果将糖尿病转化为高胰岛素性低血糖综合征,除了胰岛素瘤外,还应考虑其他成纤维细胞增生。

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