Pembrolizumab诱发甲状腺炎、肾上腺皮质炎和肾上腺炎:三重内分泌功能障碍病例。

JCEM case reports Pub Date : 2024-11-04 eCollection Date: 2024-11-01 DOI:10.1210/jcemcr/luae200
Silvia Rossi, Francesca Silvetti, Monia Bordoni, Alessandro Ciarloni, Gianmaria Salvio, Giancarlo Balercia
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引用次数: 0

摘要

免疫检查点抑制剂药物可引发自身免疫性内分泌反应,这是一种已知的副作用。已有多例免疫疗法诱发自身免疫性内分泌病的病例被描述过,但连续出现多种内分泌毒性反应的情况并不多见。一名 39 岁的转移性黑色素瘤患者开始接受 pembrolizumab 的辅助治疗。一个月后,他出现了无症状甲状腺毒症,几周后又出现了明显的甲状腺功能减退,并开始接受左甲状腺素治疗。随后,患者因可能的肾上腺功能减退症而出现中枢性肾上腺功能不全,并开始接受类固醇替代治疗。随后停止了 Pembrolizumab 治疗。几个月后,垂体功能完全恢复,但出现了原发性肾上腺功能不全,需要额外使用氟氢可的松治疗。上述临床病例是一个非常罕见的免疫疗法三重内分泌毒性病例。免疫疗法诱发的内分泌病的临床和生化表现可变且不典型;因此,有必要特别关注任何激素功能障碍的线索。
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Pembrolizumab-induced Thyroiditis, Hypophysitis and Adrenalitis: A Case of Triple Endocrine Dysfunction.

Immune checkpoint inhibitor drugs can trigger autoimmune endocrine reactions as a known side effect. Several cases of immunotherapy-induced autoimmune endocrinopathies have been described, but multiple sequential endocrine toxicities are a rare occurrence. A 39-year-old patient with metastatic melanoma started adjuvant therapy with pembrolizumab. One month later he presented with asymptomatic thyrotoxicosis and, within several weeks, overt hypothyroidism, for which he started levothyroxine therapy. Subsequently the patient developed central adrenal insufficiency due to probable hypophysitis, and steroid replacement therapy was started. Pembrolizumab therapy was then discontinued. After a few months, a full recovery of pituitary function was observed, but primary adrenal insufficiency occurred, requiring additional fludrocortisone therapy. The described clinical case is a very uncommon case of triple endocrinological toxicity from immunotherapy. The clinical and biochemical manifestations of immunotherapy-induced endocrinopathies can be variable and atypical; therefore, it is necessary to pay special attention to any clue of hormonal dysfunction.

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