Hagen G A, Bolman R M, Frank J P
Am J Med. 1975 Dec;59(6):882-8. doi: 10.1016/0002-9343(75)90482-9.
A 59 year old woman with insulin-dependent diabetes mellitus and chronic diarrhea was found to have mild steatorrhea, selective plasma IgA deficiency and adrenal insufficiency. Significant adrenal secretion of corticosteroids resulted only after prolonged stimulation with large doses of exogenous ACTH. Plasma ACTH levels were not elevated during clinical adrenal insufficiency or after metyrapone administration but did respond normally to vasopressin and insulin-induced hypoglycemia. These studies were interpreted as showing both primary adrenal insufficiency and impaired pituitary reserve for ACTH secretion in response to the feedback stimulus. No deficiency was found in secretion of other pituitary tropic hormones. Jejunal biopsy showed a lack of IgA-containing plasma cells. With cortisone replacement, diarrhea subsided and a malabsorption pattern on a film of the small bowel was no longer seen. IgA deficiency has been noted frequently with steatorrhea but rarely with diabetes and only once previously with adrenal insufficiency.
一名59岁的女性,患有胰岛素依赖型糖尿病和慢性腹泻,被发现有轻度脂肪泻、选择性血浆IgA缺乏和肾上腺功能不全。仅在大剂量外源性促肾上腺皮质激素长时间刺激后,肾上腺才会显著分泌皮质类固醇。在临床肾上腺功能不全期间或服用甲吡酮后,血浆促肾上腺皮质激素水平并未升高,但对血管加压素和胰岛素诱导的低血糖反应正常。这些研究被解释为既显示原发性肾上腺功能不全,又显示垂体对促肾上腺皮质激素分泌的储备能力受损,以应对反馈刺激。未发现其他垂体促激素分泌不足。空肠活检显示缺乏含IgA的浆细胞。使用可的松替代治疗后,腹泻减轻,小肠造影上的吸收不良模式消失。IgA缺乏症常与脂肪泻相关,但很少与糖尿病相关,此前仅曾有一次与肾上腺功能不全相关。