首页> 外文期刊>The Endocrinologist >Effective Combined Medical Treatment With Octreotide Long Acting Release (Sandostatin LAR) and Cabergoline for an Extremely Rare Pituitary Somatotroph Adenoma Producing Growth Hormone-Releasing Hormone
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Effective Combined Medical Treatment With Octreotide Long Acting Release (Sandostatin LAR) and Cabergoline for an Extremely Rare Pituitary Somatotroph Adenoma Producing Growth Hormone-Releasing Hormone

机译:奥曲肽长效释放(Sandostatin LAR)和卡麦角林的有效联合药物治疗极少见的垂体生长激素分泌型腺瘤产生生长激素释放激素。

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Combined medical treatment with long acting octreotide and cabergoline is now used with active patients with acromegaly and can reduce serum growth hormone (GH) and insulin-like growth factor-1 levels. In this article, we analyzed again the molecular aspects of the previously reported rare GH-releasing hormone (GHRH)-producing somatotroph adenoma, and introduce the effects of the combined medical treatment using octreotide LAR and cabergoline for GHRH-producing somatotroph adenoma. The present GHRH-producing somatotroph adenoma had a high Ki-67 staining index, weak, and cytoplasmic-dominant immunostaining of somatostatin receptor 2A, and no gsp mutation. This adenoma was predicted to be resistant to the medical therapy using octreotide LAR. In this extremely rare GHRH-producing pituitary somatotroph adenoma, octreotide LAR alone cannot reduce random GH and insulin-like growth factor-1 levels sufficiently, but combined medical therapy with octreotide LAR and cabergoline can reduce them into the normal range. We show that combined medical treatment with octreotide LAR and cabergoline was effective for a somatotroph adenoma that had a high proliferative potential, weak and cytoplasmic-dominant immunostaining of somatostatin receptor 2A, and no gsp mutation, and has active GH production and secretion regulated by locally generated GHRH from adenoma cell.
机译:长效奥曲肽和卡麦角林的联合药物治疗现已用于患有肢端肥大症的活跃患者,可降低血清生长激素(GH)和胰岛素样生长因子-1水平。在本文中,我们再次分析了先前报道的罕见的GH释放型生长激素腺瘤的分子方面,并介绍了使用奥曲肽LAR和卡麦角林的联合医疗对GHRH生产型生长激素腺瘤的作用。目前的产生GHRH的生长体营养腺瘤具有高的Ki-67染色指数,生长抑素受体2A的免疫染色弱且以细胞质为主,并且没有gsp突变。预测该腺瘤对使用奥曲肽LAR的药物治疗有抵抗力。在这种极为罕见的产生GHRH的垂体躯体营养腺瘤中,仅奥曲肽LAR不能充分降低GH和胰岛素样生长因子-1的随机水平,但与奥曲肽LAR和卡麦角林的联合药物治疗可将其降低至正常范围。我们显示,与奥曲肽LAR和卡麦角林联合使用的药物治疗对于生长势高,生长抑素受体2A免疫染色弱且呈细胞质占优势且无gsp突变的体细胞型腺瘤是有效的,并且其活性GH的产生和分泌受局部调节从腺瘤细胞产生GHRH。

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