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首页> 外文期刊>Hormone and Metabolic Research >Successful Treatment of Estrogen Excess in Primary Bilateral Macronodular Adrenocortical Hyperplasia with Leuprolide Acetate
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Successful Treatment of Estrogen Excess in Primary Bilateral Macronodular Adrenocortical Hyperplasia with Leuprolide Acetate

机译:用甘醇乙酸盐的原发性双侧常克罗德肾上腺皮质增生成功治疗雌激素过量

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Primary bilateral macronodular adrenocortical hyperplasia (PBMAH) is an uncommon cause of adrenal Cushing syndrome (CS) in which cortisol and occasionally other steroid hormones can be secreted under the influence of aberrantly expressed G-protein coupled receptors (GPCRs) in the adrenal cortex. We describe the unique case of a 64-year-old postmenopausal female with PBMAH whose adrenal lesions expressed luteinizing hormone receptors (LHr). She presented initially with CS and underwent right adrenalectomy; a few years later she presented with macromastia and mastodynia, possibly due to estrogen excess from her remaining left adrenocortical masses. Testing before and after treatment with quarterly leuprolide acetate therapy and immunohistochemistry on tissue and targeted sequencing of the genes of interest were performed. Tissue from the patient's right adrenal was tested for P450 aromatase (CYP19A1) and LHr expression; both were expressed throughout the hyperplastic cortex, although expression was more intense in the adenomatous areas. Targeted sequencing revealed a pathogenic PDE11A mutation, as well as variants in the ARMC5 and INHA genes. PDE11A expression was decreased in the adenoma but there was no loss of heterozygosity for the PDE11A locus. Because of the clinical presentation and LHr expression, quarterly leuprolide acetate therapy was started. Shortly after initiation of therapy, the patient reported decreased breast size and pain; she remains well controlled to date, after 10 years of treatment. This is the first description of a patient with PBMAH presenting with severe macromastia and mastodynia from what appears to be excess estrogen production from her adrenal tumor. The patient had a long-lasting response to chronic leuprolide acetate treatment, showing that drug therapy exploiting the aberrant receptor expression in PBMAH is possible even in the absence of cortisol overproduction.
机译:原发性双侧常规肾上腺皮质增生(PBMAH)是肾上腺囊型综合征(CS)的罕见原因,其中皮质醇和偶尔其他类固醇激素可以在肾上腺皮质中的异常表达的G蛋白偶联受体(GPCR)的影响下分泌。我们用PBMAH描述了一个64岁的绝经女性女性的独特案例,其肾上腺病变表达了叶黄素激素受体(LHR)。她最初用CS和接受右肾切除术呈现;几年后,她介绍了大分子和乳房,可能是由于她剩下的左肾上腺皮质肿块的雌激素过量。进行季耳丙酯治疗和免疫组织化学治疗前后的测试,并进行了有趣基因的组织和靶向测序。对患者的右肾上腺的组织进行P450芳香酶(CYP19A1)和LHR表达式测试;两者在整个增生皮层中表达,尽管表达在腺瘤区域更强烈。靶向测序揭示了致病PDE11a突变,以及ARMC5和INHA基因中的变体。在腺瘤中,PDE11a表达减少,但PDE11a基因座没有杂合子损失。由于临床介绍和LHR表达,开始了季耳丙酮治疗。在开始治疗后不久,患者报告乳房大小和疼痛减少;经过10年的治疗后,她仍然受到良好的控制。这是PBMAH患者患有严重的大分子和Mastodynia的患者的第一次描述,从肾上腺肿瘤中似乎过量雌激素产生。患者对慢性果冻乙酸酯治疗具有持久的反应,表明,即使在没有皮质醇过度生产的情况下,也可以利用PBMAH中异常受体表达的药物治疗。

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