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在轻度和偶发性库欣综合征患者中,评估高皮质醇血症的检测呈高发正常,这表明库欣综合征的诊断和排除范式需要进行多项检测。

High prevalence of normal tests assessing hypercortisolism in subjects with mild and episodic Cushing's syndrome suggests that the paradigm for diagnosis and exclusion of Cushing's syndrome requires multiple testing.

机构信息

Division of Endocrinology, Metabolism, and Molecular Medicine, Charles Drew University of Medicine and Science, Los Angeles, CA 90059, USA.

出版信息

Horm Metab Res. 2010 Nov;42(12):874-81. doi: 10.1055/s-0030-1263128. Epub 2010 Aug 27.

Abstract

Many Endocrinologists believe that a single determination of eucortisolism or a single demonstration of appropriate suppression to dexamethasone excluded Cushing's syndrome, except in what was previously thought to be the rare patient with episodic or periodic Cushing's syndrome. We hypothesize that episodic Cushing's syndrome is relatively common and a single test assessing hypercortisolism may not be sufficient to accurately rule out or diagnose Cushing's syndrome and retrospectively examined the number of normal and abnormal tests assessing hypercortisolism performed on multiple occasions in 66 patients found to have mild and/or episodic Cushing's syndrome compared to a similar group of 54 patients evaluated for, but determined not to have Cushing's syndrome. We found that 65 of the 66 patients with Cushing's syndrome had at least one normal test of cortisol status and most patients had several normal tests. The probability of having Cushing's syndrome when one test was negative was 92% for 23:00 h salivary cortisol, 88% for 24-h UFC, 86% for 24-h 17OHS, and 54% for nighttime plasma cortisol. These results demonstrated that episodic hypercortisolism is highly prevalent in subjects with mild Cushing's syndrome and no single test was effective in conclusively diagnosing or excluding the condition. Rather, the paradigm for the diagnosis should be a careful history and physical examination and in those patients in whom mild Cushing's syndrome/disease is strongly suspected, multiple tests assessing hypercortisolism should be performed on subsequent occasions, especially when the patient is experiencing signs and symptoms of short-term hypercortisolism.

摘要

许多内分泌学家认为,单次检测皮质醇正常或单次地塞米松抑制试验结果正常,即可排除库欣综合征,除非患者先前被认为是偶发性或周期性库欣综合征的罕见病例。我们假设偶发性库欣综合征较为常见,单次评估皮质醇过多的检查可能不足以准确排除或诊断库欣综合征。我们回顾性分析了 66 例轻度和/或偶发性库欣综合征患者多次检查皮质醇状态的结果,与 54 例评估但未确诊库欣综合征的患者进行了比较。我们发现,66 例库欣综合征患者中有 65 例至少有一次皮质醇状态的正常检查,大多数患者有多次正常检查。当一次检查结果为阴性时,23:00 唾液皮质醇、24 小时 UFC、24 小时 17-羟皮质类固醇和夜间血浆皮质醇诊断库欣综合征的概率分别为 92%、88%、86%和 54%。这些结果表明,轻度库欣综合征患者中偶发性皮质醇过多症非常普遍,没有单一检查可以有效确诊或排除该疾病。相反,诊断的范例应该是仔细的病史和体格检查,对于那些强烈怀疑患有轻度库欣综合征/疾病的患者,应在随后的时间进行多次评估皮质醇过多的检查,尤其是当患者出现短期皮质醇过多的症状和体征时。

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