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两例醛固酮瘤患者中地塞米松不可抑制的皮质醇

Dexamethasone-nonsuppressible cortisol in two cases with aldosterone-producing adenoma.

作者信息

Imai T, Seo H, Murata Y, Funahashi H, Satoh Y, Sasano H, Matsui N, Takagi H

机构信息

Department of Endocrinology and Metabolism, Nagoya University, Japan.

出版信息

J Clin Endocrinol Metab. 1991 Mar;72(3):575-81. doi: 10.1210/jcem-72-3-575.

Abstract

Forty-one patients with aldosterone-producing adenoma (APA) were subjected to a dexamethasone suppression test (DST) before surgery. Serum cortisol and urinary excretion of 17-hydroxycorticosteroids were suppressed by dexamethasone in 39 patients [DST(+)]. In two patients (cases A and B), they were not suppressed [DST(-)]. Clinical manifestations of the two DST(-) patients were similar to those of DST(+) patients. Hypertension, hypokalemia, high serum aldosterone levels, and suppressed PRA were found in all of the patients. The cut surfaces of the adenomas from all of the patients, including cases A and B, were golden yellow, which is typical of APA. However, atrophies of the adjacent normal tissues were evident exclusively in the two DST(-) patients. After removal of the affected adrenals, the serum cortisol level was suppressed by dexamethasone in one of the DST(-) patients (case B). These findings suggested autonomous cortisol production by APA. To evaluate whether cortisol could be produced from the adenoma tissue, the presence of several steroidogenic enzymes was studied by immunohistochemistry and mRNA analysis in the adenomas and the adjacent nonneoplastic adrenals from the 2 DST(-) and 5 DST(+) patients. Immunohistochemical analysis demonstrated that steroidogenic enzymes were expressed in APA tumor tissues from both DST(-) and DST(+) patients. In both groups, mRNAs coding steroidogenic enzymes were present not only in the nonneoplastic but also in the tumor tissues. Quantitative analysis of the mRNA levels revealed that in the adrenals from DST(+) patients, the mRNAs were more abundant in nonneoplastic tissue than in tumor tissue. However, in those from DST(-) cases, the mRNAs were much more abundant in the tumor tissues than in the nonneoplastic tissues. These results indicate that tumor cells of the two DST(-) patients autonomously synthesized not only aldosterone but also cortisol. The diameters of the tumors from the two DST(-) patients exceeded 3 cm, while those from other DST(+) patients were smaller. In patients with large APA, adrenal insufficiency should be anticipated upon removal of the tumor.

摘要

41例醛固酮瘤(APA)患者在手术前接受了地塞米松抑制试验(DST)。39例患者的血清皮质醇和17-羟皮质类固醇的尿排泄受到地塞米松抑制[DST(+)]。2例患者(A和B病例)未受抑制[DST(-)]。这2例DST(-)患者的临床表现与DST(+)患者相似。所有患者均有高血压、低钾血症、高血清醛固酮水平和肾素活性受抑制。包括A和B病例在内的所有患者的腺瘤切面均为金黄色,这是APA的典型表现。然而,仅在这2例DST(-)患者中,相邻正常组织有明显萎缩。切除患侧肾上腺后,1例DST(-)患者(B病例)的血清皮质醇水平受到地塞米松抑制。这些发现提示APA可自主产生皮质醇。为评估腺瘤组织是否能产生皮质醇,通过免疫组织化学和mRNA分析研究了2例DST(-)和5例DST(+)患者的腺瘤及相邻非肿瘤性肾上腺中几种类固醇生成酶的存在情况。免疫组织化学分析表明,DST(-)和DST(+)患者的APA肿瘤组织中均表达类固醇生成酶。在两组中,编码类固醇生成酶的mRNA不仅存在于非肿瘤组织中,也存在于肿瘤组织中。mRNA水平的定量分析显示,在DST(+)患者的肾上腺中,非肿瘤组织中的mRNA比肿瘤组织中更丰富。然而,在DST(-)病例中,肿瘤组织中的mRNA比非肿瘤组织中丰富得多。这些结果表明,这2例DST(-)患者的肿瘤细胞不仅自主合成醛固酮,还合成皮质醇。这2例DST(-)患者的肿瘤直径超过3 cm,而其他DST(+)患者的肿瘤较小。对于大APA患者,切除肿瘤后应预计会出现肾上腺功能不全。

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