Giustina A, Candrina R, Cimino A, Romanelli G
Cattedra di Patologia Speciale Medica, Università di Brescia, Italy.
J Endocrinol Invest. 1988 May;11(5):375-7. doi: 10.1007/BF03349058.
A 45-year-old man with type I diabetes mellitus of 25-yr duration and well controlled by conventional insulin therapy developed an isolated adrenocorticotropic hormone (ACTH) deficiency. He presented with a 3-month history of weight loss, weakness, anorexia and persistent tendency to hypoglycemia that he had never experienced before. Basal and dynamic endocrine testing disclosed absent cortisol secretion caused by an isolated ACTH deficiency due to a primary pituitary defect. Corticosteroid replacement therapy allowed again a good glycometabolic control. The possible causes of hypoglycemia in insulin-treated diabetes and the pathogenetic basis of the reported association are discussed.
一名45岁男性,患1型糖尿病25年,一直通过传统胰岛素治疗得到良好控制,现出现孤立性促肾上腺皮质激素(ACTH)缺乏。他有3个月体重减轻、乏力、厌食及持续低血糖倾向的病史,而低血糖倾向是他以前从未经历过的。基础及动态内分泌检查显示,由于原发性垂体缺陷导致孤立性ACTH缺乏,引起皮质醇分泌缺失。皮质类固醇替代治疗再次使血糖代谢得到良好控制。本文讨论了胰岛素治疗的糖尿病患者发生低血糖的可能原因以及所报道关联的发病机制基础。