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偶然发现肾上腺腺瘤导致的可能的库欣综合征前期。

Possible pre-Cushing's syndrome due to an adrenal adenoma incidentally discovered.

作者信息

Tsuboi Y, Ishikawa S, Fujisawa G, Okada K, Saito T

机构信息

Department of Medicine, Jichi Medical School, Tochigi, Japan.

出版信息

Endocr J. 1995 Aug;42(4):509-16. doi: 10.1507/endocrj.42.509.

Abstract

We demonstrated the functional evaluation of adrenal incidentaloma in 8 patients who had no abnormal finding associated with Cushing's syndrome. Adrenal tumors were incidentally discovered by abdominal echogram in 5 patients and by computed tomography (CT) in 3 patients. Serum cortisol levels and urinary excretion of 17-hydroxycorticosteroids (17-OHCS) were within normal limits in four of 8 patients. Urinary excretion of free cortisol was also within normal limits except for patient 8. Urinary excretion of 17-OHCS, however, was not suppressed by dexamethasone administration in five of 8 patients. Excretion of urinary 17-OHCS did not increase in response to metyrapone in 3 of 4 dexamethasone-insuppressible patients, but increased in 3 dexamethasone-suppressible ones. Serum cortisol increased in response to exogenous ACTH in all 6 patients examined. 131I-Adosterol accumulation was found in only the tumor side in 7 patients and bilaterally in one patient. Adrenalectomy was done in 7 patients, and microscopic findings showed adrenocortical adenoma. Serum cortisol was significantly suppressed in response to dexamethasone in the post-operative stage in all 7 patients examined. These results indicate that these adrenal incidentalomas seem to have a cortisol over-production which is dexamethasone-insuppressible and ACTH-dependent, and that they can be classified as "Pre-Cushing's Syndrome."

摘要

我们对8例无库欣综合征相关异常发现的肾上腺偶发瘤患者进行了功能评估。5例患者通过腹部超声偶然发现肾上腺肿瘤,3例患者通过计算机断层扫描(CT)发现。8例患者中有4例血清皮质醇水平和尿17-羟皮质类固醇(17-OHCS)排泄量在正常范围内。除患者8外,尿游离皮质醇排泄量也在正常范围内。然而,8例患者中有5例尿17-OHCS排泄量未被地塞米松抑制。在4例地塞米松抑制试验无反应的患者中,3例对甲吡酮的反应尿17-OHCS排泄量未增加,但在3例地塞米松可抑制的患者中增加。在所有6例接受检查的患者中,血清皮质醇对外源性促肾上腺皮质激素(ACTH)有反应性增加。7例患者仅在肿瘤侧发现131I-阿多甾醇积聚,1例患者双侧发现。7例患者接受了肾上腺切除术,显微镜检查结果显示为肾上腺皮质腺瘤。在所有7例接受检查的患者术后阶段,血清皮质醇对地塞米松有明显抑制反应。这些结果表明,这些肾上腺偶发瘤似乎存在地塞米松抑制试验无反应且依赖ACTH的皮质醇过度分泌,并且它们可被归类为“库欣综合征前期”。

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