A case of asymptomatic cortisol producing adrenal adenoma.

M Noritake, K Morimoto, H Kosano, Y Nemoto, N Kugai, M Takao, M Murai, S Tamai, K Tanaka, N Nagata
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引用次数: 12

Abstract

We describe a man without the clinical findings of Cushing's syndrome, but who harbored an incidentally found cortisol-producing adrenal adenoma. On adrenal 131I-adsterol imaging, there was good uptake to the nodule, but no visualization of the contralateral adrenal. No abnormalities were found in the basal plasma cortisol, ACTH, urinary free cortisol and 17OHCS. However, dynamic hormone assessment revealed the existence of abnormal cortisol secretion: no suppression to dexamethasone, incomplete response to human corticotropin-releasing hormone, and lack of diurnal variation in plasma cortisol. Left adrenalectomy was performed with the diagnosis of cortisol-producing adrenal tumor. The pathological finding was an adrenal adenoma, and the perifusion of the excised tissues revealed a negligible response of the tumor tissue to ACTH though the residual normal cortex responded. Postoperative course was uneventful without replacement therapy with cortisol. It is suggested that the tumor autonomously produced a small amount of cortisol not only insufficient to provide clinical Cushing's syndrome, but also to provide typical suppression of hypothalamo-pituitary corticotroph-adrenal system.

无症状皮质醇产生肾上腺腺瘤1例。
我们描述了一个没有库欣综合征临床表现的人,但他偶然发现了产生皮质醇的肾上腺腺瘤。肾上腺131I-adsterol显像显示结节摄取良好,但对侧肾上腺未见明显。基础血浆皮质醇、ACTH、尿游离皮质醇、17OHCS均未见异常。然而,动态激素评估显示存在异常皮质醇分泌:对地塞米松无抑制,对人促肾上腺皮质激素释放激素反应不完全,血浆皮质醇缺乏日变化。诊断为产生皮质醇的肾上腺肿瘤,行左肾上腺切除术。病理发现是肾上腺腺瘤,切除组织的浸润显示肿瘤组织对ACTH的反应可以忽略不计,尽管残余的正常皮质有反应。术后无皮质醇替代治疗。提示肿瘤自主产生的少量皮质醇不仅不足以提供临床库欣综合征,而且还提供了典型的下丘脑-垂体促皮质-肾上腺系统抑制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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