Isolated Adrenocorticotropic Hormone Deficiency Associated with Sintilimab in the Treatment of Lung Adenocarcinoma: A Case Report and Literature Review.

IF 1.8 4区 医学 Q4 ENDOCRINOLOGY & METABOLISM
Zehui Liu, Qiang Ma, Sha Ma, Mengru Yang, Haowei Zhang, Wenzhuo Zhu, Rui Han
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引用次数: 0

Abstract

Isolated adrenocorticotropic hormone (ACTH) deficiency, a rare condition associated with immune checkpoint inhibitors, can manifest with symptoms such as fatigue, poor appetite, dizziness, hypotension, and hyponatremia. We present a case of a 52-year-old Chinese woman with stage IB lung adenocarcinoma who developed these symptoms after 8 months of treatment with sintilimab. Laboratory tests revealed hyponatremia, low ACTH and cortisol levels, and thyrotoxicosis. Imaging studies showed a Rathke's cleft cyst in the pituitary gland but normal adrenal glands. The patient was diagnosed with isolated ACTH deficiency and thyroid dysfunction and prescribed prednisone as replacement therapy, which improved her symptoms despite persistently low ACTH levels. This case highlights the importance of early diagnosis and treatment of immune checkpoint inhibitor-related endocrine disorders and provides insights into their management to enhance clinical practice and outcomes.

孤立性促肾上腺皮质激素缺乏与辛替单抗治疗肺腺癌:1例报告和文献综述。
孤立性促肾上腺皮质激素(ACTH)缺乏是一种与免疫检查点抑制剂相关的罕见疾病,可表现为疲劳、食欲不振、头晕、低血压和低钠血症等症状。我们报告一例52岁的中国女性IB期肺腺癌患者,在接受辛替单抗治疗8个月后出现上述症状。实验室检查显示低钠血症,低ACTH和皮质醇水平,甲状腺毒症。影像学检查显示脑垂体有拉克氏裂隙囊肿,但肾上腺正常。患者被诊断为孤立性ACTH缺乏和甲状腺功能障碍,处方强的松作为替代治疗,尽管持续低ACTH水平,但患者的症状得到改善。本病例强调了免疫检查点抑制剂相关内分泌紊乱的早期诊断和治疗的重要性,并提供了对其管理的见解,以加强临床实践和结果。
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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来源期刊
Endocrine Research
Endocrine Research 医学-内分泌学与代谢
CiteScore
4.30
自引率
0.00%
发文量
10
审稿时长
>12 weeks
期刊介绍: This journal publishes original articles relating to endocrinology in the broadest context. Subjects of interest include: receptors and mechanism of action of hormones, methodological advances in the detection and measurement of hormones; structure and chemical properties of hormones. Invitations to submit Brief Reviews are issued to specific authors by the Editors.
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