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首页> 外文期刊>Endocrine journal >Metyrapone-responsive ectopic ACTH-secreting pheochromocytoma with a vicious cycle via a glucocorticoid-driven positive-feedback mechanism
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Metyrapone-responsive ectopic ACTH-secreting pheochromocytoma with a vicious cycle via a glucocorticoid-driven positive-feedback mechanism

机译:Metyrapone反应性异位促肾上腺皮质激素分泌性嗜铬细胞瘤通过糖皮质激素驱动的正反馈机制形成恶性循环

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In ectopic ACTH-secreting pheochromocytoma, combined ACTH-driven hypercortisolemia and hypercatecholaminemia are serious conditions, which can be fatal if not diagnosed and managed appropriately, especially when glucocorticoid-driven positive feedback is suggested with a high ACTH/cortisol ratio. A 46-year-old man presented with headache, rapid weight loss, hyperhidrosis, severe hypertension and hyperglycemia without typical Cushingoid appearance. Endocrinological examinations demonstrated elevated plasma and urine catecholamines, serum cortisol and plasma ACTH. Moreover, his ACTH/cortisol ratio and catecholamine levels were extremely high, suggesting catecholamine-dominant ACTH-secreting pheochromocytoma. Computed tomography revealed a large right adrenal tumor. 18F-FDG positron emission tomography showed uptake in the area of the adrenal tumor, while 123I-metaiodobenzylguanidine scintigraphy showed no accumulation. His plasma ACTH level paradoxically became elevated after a dexamethasone suppression test. After metyrapone administration, not only serum cortisol but also plasma ACTH levels were exponentially decreased almost in parallel, suggesting a glucocorticoid-driven positive-feedback regulation in this rapidly exacerbated ectopic ACTH-producing pheochromocytoma. Interestingly enough, plasma catecholamine levels were also decreased by metyrapone, although they remained extremely high. He became severely dehydrated due to hypoadrenalism requiring hydrocortisone supplementation. His clinical signs and symptoms were improved, and right adrenalectomy was performed uneventfully, resulting in complete remission of pheochromocytoma and Cushing’s syndrome. A glucocorticoid-driven positive-feedback regulation in this ectopic ACTH-secreting pheochromocytoma created a vicious cycle with rapid exacerbation of both hypercortisolemia and hypercatecholaminemia with extremely elevated plasma ACTH level. Metyrapone was clinically effective to stop this vicious cycle; nonetheless, great care must be taken to avoid hypoadrenalism especially when hypercatecholaminemia remained.
机译:在异位ACTH分泌型嗜铬细胞瘤中,合并的ACTH驱动的高皮质醇血症和高儿茶酚胺血症是严重的疾病,如果不加以正确诊断和处理,则可能是致命的,特别是当糖皮质激素驱动的阳性反馈被认为具有较高的ACTH /皮质醇比率时。一名46岁的男子表现出头痛,体重迅速减轻,多汗症,严重的高血压和高血糖症,而没有典型的库欣格样外观。内分泌检查显示血浆和尿中儿茶酚胺,血清皮质醇和血浆ACTH升高。此外,他的ACTH /皮质醇比率和儿茶酚胺水平极高,表明儿茶酚胺占主导地位的分泌ACTH的嗜铬细胞瘤。计算机断层扫描显示右肾上腺肿瘤较大。 18F-FDG正电子发射断层显像显示在肾上腺肿瘤区域摄取,而123I-甲氧苄基胍闪烁显像显示无积聚。地塞米松抑制试验后,他的血浆ACTH水平反常升高。服用甲吗啡酮后,不仅血清皮质醇而且血浆ACTH水平几乎同时呈指数下降,这表明在这种迅速加剧的异位ACTH产生性嗜铬细胞瘤中,糖皮质激素驱动的正反馈调节。有趣的是,甲吡酮可降低血浆儿茶酚胺水平,尽管仍然很高。由于肾上腺皮质功能减退需要补充氢化可的松,他严重脱水。他的临床体征和症状得到改善,右肾上腺切除术进行得很顺利,导致嗜铬细胞瘤和库欣综合征完全缓解。在这种分泌ACTH的异位嗜铬细胞瘤中,糖皮质激素驱动的正反馈调节产生了恶性循环,高皮质醇血症和高儿茶酚胺症迅速加重,血浆ACTH水平显着升高。 Metyrapone在临床上可有效阻止这种恶性循环;然而,必须特别注意避免肾上腺皮质功能低下,特别是当剩余儿茶酚胺过多时。

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