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使用和不使用促肾上腺皮质激素释放激素的岩下窦采血用于库欣综合征的鉴别诊断

Petrosal sinus sampling with and without corticotropin-releasing hormone for the differential diagnosis of Cushing's syndrome.

作者信息

Oldfield E H, Doppman J L, Nieman L K, Chrousos G P, Miller D L, Katz D A, Cutler G B, Loriaux D L

机构信息

Surgical Neurology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Md 20892.

出版信息

N Engl J Med. 1991 Sep 26;325(13):897-905. doi: 10.1056/NEJM199109263251301.

Abstract

BACKGROUND

Measurement of adrenocorticotropin levels in plasma from the inferior petrosal sinuses of patients with Cushing's syndrome can distinguish adrenocorticotropin-secreting pituitary tumors (Cushing's disease) from other causes of the syndrome, principally ectopic adrenocorticotropin secretion from an occult tumor. However, it is unknown whether such measurement consistently identifies patients with Cushing's disease and whether testing with corticotropin-releasing hormone (CRH) enhances the value of the procedure.

METHODS

We prospectively studied 281 patients with Cushing's syndrome to evaluate the diagnostic efficacy of the procedure. Bilateral sampling was successfully accomplished in 278 patients, with no major morbidity; 262 of these patients underwent sampling before and after administration of ovine CRH. The adrenocorticotropin levels in the samples were used to calculate the ratio of the concentration in plasma from the inferior petrosal sinuses to the concentration in peripheral-blood plasma (the IPS:P ratio).

RESULTS

The diagnosis of 246 patients was confirmed surgically as Cushing's disease in 215, as ectopic adrenocorticotropin syndrome in 20, and as primary adrenal disease in 11. An IPS:P ratio greater than or equal to 2.0 in basal samples identified 205 of the 215 patients with Cushing's disease (sensitivity, 95 percent), with no false positive results (specificity, 100 percent). A peak IPS:P ratio greater than or equal to 3.0 after CRH administration identified all 203 of the patients with Cushing's disease who received CRH (sensitivity, 100 percent), with no false positive results (specificity, 100 percent). The sensitivity was much lower when the adrenocorticotropin concentrations in the samples from one sinus were considered alone. In patients with Cushing's disease a difference of greater than or equal to 1.4-fold between the concentrations in the two sinuses (the adrenocorticotropin gradient) predicted the location of the microadenoma in 68 percent of 104 patients during basal sampling and in 71 percent of 105 patients after CRH administration.

CONCLUSIONS

Simultaneous bilateral sampling of plasma from the inferior petrosal sinuses, with the adjunctive use of CRH, distinguishes patients with Cushing's disease from those with ectopic adrenocorticotropin secretion with high diagnostic accuracy.

摘要

背景

测量库欣综合征患者岩下窦血浆中的促肾上腺皮质激素水平,可将分泌促肾上腺皮质激素的垂体肿瘤(库欣病)与该综合征的其他病因区分开来,主要是隐匿肿瘤分泌的异位促肾上腺皮质激素。然而,尚不清楚这种测量能否始终如一地识别出库欣病患者,以及促肾上腺皮质激素释放激素(CRH)试验是否能提高该检查的价值。

方法

我们对281例库欣综合征患者进行了前瞻性研究,以评估该检查的诊断效能。278例患者成功完成双侧采样,无严重并发症;其中262例患者在注射羊CRH前后进行了采样。样本中的促肾上腺皮质激素水平用于计算岩下窦血浆浓度与外周血血浆浓度之比(IPS:P比值)。

结果

246例患者的诊断经手术证实,215例为库欣病,20例为异位促肾上腺皮质激素综合征,11例为原发性肾上腺疾病。基础样本中IPS:P比值大于或等于2.0可识别出215例库欣病患者中的205例(敏感性为95%),无假阳性结果(特异性为100%)。注射CRH后峰值IPS:P比值大于或等于3.0可识别出所有接受CRH的203例库欣病患者(敏感性为100%),无假阳性结果(特异性为100%)。单独考虑一个窦样本中的促肾上腺皮质激素浓度时,敏感性要低得多。在库欣病患者中,两个窦浓度之间的差异大于或等于1.4倍(促肾上腺皮质激素梯度)在基础采样时可预测104例患者中68%的微腺瘤位置,注射CRH后可预测105例患者中71%的微腺瘤位置。

结论

岩下窦血浆同时双侧采样并辅助使用CRH,可将库欣病患者与异位促肾上腺皮质激素分泌患者区分开来,诊断准确性高。

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