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A Case of Transient ACTH Deficiency Associated with Polymyalgia Rheumatica

机译:风湿性多肌痛伴一过性ACTH缺乏症一例

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摘要

We report a case of 79-year-old man, who was diagnosed to have transient ACTH deficiency associated with polymyalgia rheumatica (PMR). The patient presented with sudden onset bilateral shoulder pain, which was gradually aggravated. Plasma ACTH was undetectable, and both serum cortisol and urinary 17-OHCS were very low. Other pituitary hormones were normal, suggesting that hypothalamo-pituitary-adrenal (HPA) axis is selectively damaged. However, within several weeks, plasma ACTH returned to normal, and showed a normal increase response to corticotropin-releasing hormone stimulation test. These results indicated that ACTH deficiency was only transient. After hydrocortisone (10 mg/day) was administered, his symptoms became suddenly improved. Based on those results and clinical course, ie, elevated erythrocyte sedimentation rate, negative rheumatoid factor and the typical symptoms, which showed improvement to glulcocorticoid therapy, the final diagnosis was PMR, which was associated with transient ACTH deficiency.This is the first report of a case of PMR, in which the HPA axis was examined in its very acute phase. It was demonstrated that the case was associated with the transient adrenocortical hypofunction, which was recovered during a short time. It is therefore possible that PMR may show a different responsiveness of HPA axis depending on its phases.
机译:我们报告一例79岁的男子,被诊断患有短暂性ACTH缺乏症,伴有风湿性多肌痛(PMR)。该患者突然发作双侧肩痛,并逐渐加重。血浆ACTH不可检测,血清皮质醇和尿17-OHCS都非常低。其他垂体激素正常,提示下丘脑-垂体-肾上腺(HPA)轴被选择性破坏。然而,在几周内,血浆ACTH恢复正常,并显示出对促肾上腺皮质激素释放激素刺激试验的正常增加反应。这些结果表明ACTH缺乏症只是短暂的。服用氢化可的松(10毫克/天)后,他的症状突然好转。根据这些结果和临床过程,即红细胞沉降率升高,类风湿因子阴性和典型症状表现出对糖皮质激素治疗的改善,最终诊断为PMR,这与短暂性ACTH缺乏有关。 PMR的情况,其中HPA轴处于非常急性的阶段。事实证明,该病例与短暂性肾上腺皮质功能减退有关,并在短时间内恢复。因此,PMR可能会根据其相位表现出不同的HPA轴响应性。

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