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首页> 外文期刊>Therapeutics and Clinical Risk Management >Retention of aberrant cortisol secretion in a patient with bilateral macronodular adrenal hyperplasia after unilateral adrenalectomy
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Retention of aberrant cortisol secretion in a patient with bilateral macronodular adrenal hyperplasia after unilateral adrenalectomy

机译:单侧肾上腺切除术后双侧大结节性肾上腺增生患者异常皮质醇分泌的保留

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摘要

Aberrant cortisol secretion responses after exogenous stimuli such as upright posture, eating a mixed meal or receiving agents influencing aberrant G-protein-coupled receptors in adrenal glands, are often observed in patients with bilateral macronodular adrenal hyperplasia (BMAH). However, little is known about whether this aberrant response is retained after unilateral adrenalectomy. Here, we describe a 61-year-old postmenopausal Japanese woman with unsatisfactorily controlled hypertension who was referred to us for further investigation due to her pre-obesity characteristics (body mass index 28.4 kg/msup2/sup). Cushing’s signs and serum cortisol at 16.2 μg/dL with undetectable adrenocorticotropic hormone indicated adrenal Cushing’s syndrome. Adrenal imaging revealed bilaterally enlarged adrenal glands with 131-I adosterol uptake; hence, BMAH was diagnosed. Preoperatively, in vivo screening for aberrant adrenal receptors revealed an aberrant response of cortisol secretion on metoclopramide challenge. The patient underwent unilateral adrenalectomy; thereafter, glucocorticoid replacement therapy was reduced to hydrocortisone 15 mg/day at postoperative day 6. Fasting morning serum cortisol level measured at postoperative day 8 was 2.96 μg/dL, suggesting adrenal insufficiency. However, following metoclopramide administration serum cortisol level rose to 19.7 μg/dL, indicating potential efficient adrenal function. Aberrant cortisol secretory capacity was thus preserved in BMAH, even in a state of adrenal insufficiency after unilateral adrenalectomy. Caution should be exercised when assessing the hypothalamus-pituitary-adrenal axis, because in this patient, a high cortisol level did not guarantee appropriate adrenal function when the patient was challenged by exogenous stimuli.
机译:在患有双侧大结节性肾上腺增生(BMAH)的患者中,经常观察到外源刺激(例如直立姿势,进食混合餐或接受影响肾上腺G蛋白偶联受体异常的药物)后皮质醇分泌异常。但是,对于单侧肾上腺切除术后是否仍保留这种异常反应知之甚少。在这里,我们描述了一位61岁的绝经后高血压控制不佳的日本女性,由于其肥胖前期特征(体重指数28.4 kg / m 2 )而被转介给我们进行进一步调查。库欣的体征和血清皮质醇水平为16.2μg/ dL,且未检测到促肾上腺皮质激素,表明库欣综合征。肾上腺成像显示双侧肾上腺肿大,摄取131-I肾上腺素。因此,诊断为BMAH。术前,体内对异常肾上腺受体的筛查显示,甲氧氯普胺激发后皮质醇分泌异常。患者进行了单侧肾上腺切除术;此后,在术后第6天将糖皮质激素替代疗法减至氢化可的松15 mg /天。术后8天空腹早上血清皮质醇水平为2.96μg/ dL,提示肾上腺皮质功能不全。但是,服用甲氧氯普胺后,血清皮质醇水平升至19.7μg/ dL,表明潜在的有效肾上腺功能。因此,即使在单侧肾上腺切除术后的肾上腺皮质功能不全的状态下,BMAH中仍保留了异常的皮质醇分泌能力。评估下丘脑-垂体-肾上腺轴时应谨慎,因为在该患者中,当患者受到外源性刺激时,高皮质醇水平不能保证其适当的肾上腺功能。

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