Potential pitfalls in diagnosis of immunotherapy-induced hypothalamic-pituitary-adrenal axis abnormalities: a clinical case.

Yixi Bi, Safwaan Adam, Viktoria Chatzimavridou, Paul Lorigan, Yinglai Huang
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引用次数: 2

Abstract

Summary: Short synacthen tests (SST) are frequently used for assessing adrenocorticotropin hormone (ACTH) deficiency. In this study, we present the case of a 53-year-old man receiving immunotherapy for metastatic melanoma, who subsequently developed immune checkpoint inhibitor (ICI)-induced hypothyroidism and was investigated for the presence of ICI-induced hypocortisolaemia on different occasions. Despite two reassuring SSTs, he subsequently developed clinical and biochemical evidence of ACTH deficiency. The ACTH on local measurement was not conclusive in keeping with ICI-related ACTH deficiency but when repeated using an alternative assay confirmed the diagnosis. The case illustrates the evolution of ACTH deficiency and exposes the potential pitfalls of screening strategies. Two important lessons may be gleaned from this case: (i) SSTs can be normal in early cases of secondary adrenal insufficiency, for example, hypophysitis due to adrenal reserve and (ii) when there is mismatch between the clinical and biochemical presentation, the ACTH should be repeated using a different assay.

Learning points: Short synacthen tests, useful for ruling out adrenalitis and primary adrenal failure, may be normal in early adrenocorticotrophic hormone deficiency and secondary adrenal failure due to residual adrenal reserve.If clinical suspicion of adrenal insufficiency persists despite an initial satisfactory SST, it is important to recognise the need for re-assessment of cortisol levels.Insulin tolerance test remains a useful tool in the investigation of secondary adrenal insufficiency.Levothyroxine replacement may accelerate the metabolism of cortisol in cases of concurrent hypothyroidism and hypoadrenalism, and therefore, glucocorticoid replacement must precede levothyroxine treatment, to avoid adrenal crisis.The prevalence of immunotherapy-related endocrinopathies is likely to increase with increasing use of ICI and it is crucial that clinicians are alert to their subtle symptoms.

Abstract Image

Abstract Image

诊断免疫治疗引起的下丘脑-垂体-肾上腺轴异常的潜在缺陷:一个临床病例。
摘要:短促肾上腺皮质激素试验(SST)常用于评估促肾上腺皮质激素(ACTH)缺乏。在这项研究中,我们报告了一名53岁的男性接受转移性黑色素瘤免疫治疗的病例,他随后发展为免疫检查点抑制剂(ICI)诱导的甲状腺功能减退症,并在不同场合调查了ICI诱导的低皮质醇血症的存在。尽管有两次令人放心的sst,但他随后发现了ACTH缺乏症的临床和生化证据。ACTH在局部测量是不确定的,在保持与ici相关的ACTH缺乏症,但当重复使用替代测定证实诊断。该病例说明了ACTH缺乏症的演变,并暴露了筛查策略的潜在缺陷。从这个病例中可以得到两个重要的教训:(i)在继发性肾上腺功能不全的早期病例中,SSTs可能是正常的,例如,肾上腺储备引起的垂体炎;(ii)当临床和生化表现不匹配时,ACTH应该使用不同的检测方法重复。学习要点:短synacthen试验可用于排除肾上腺炎和原发性肾上腺衰竭,在早期促肾上腺皮质激素缺乏和由于残留肾上腺储备导致的继发性肾上腺衰竭中可能是正常的。如果临床怀疑肾上腺功能不全,尽管最初的SST满意,重要的是要认识到需要重新评估皮质醇水平。胰岛素耐量试验仍然是研究继发性肾上腺功能不全的有效工具。在合并甲状腺功能减退和肾上腺功能减退的情况下,左旋甲状腺素替代可能会加速皮质醇的代谢,因此,糖皮质激素替代必须先于左旋甲状腺素治疗,以避免肾上腺危机。免疫治疗相关内分泌疾病的患病率可能随着ICI使用的增加而增加,临床医生对其细微症状保持警惕至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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