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Updated: Jun 25, 2025

Preparation of Mouse Pituitary Immunogen for the Induction of Experimental Autoimmune Hypophysitis
Published on: December 17, 2010
Immune checkpoint inhibitor-induced hypophysitis with transient ACTH-dependent hypercortisolism.
Fatima Abdullah AlRubaish1, Nisha Gupta2, Meng Zhu Shi3
1Department of Internal Medicine, Imam Abdulrahman Bin Faisal University, Dammam, Eastern Province, Saudi Arabia fatima.alrubaish@mail.mcgill.ca.
Immune checkpoint inhibitors can cause transient ACTH-dependent hypercortisolism, leading to secondary adrenal insufficiency. Vigilant monitoring is crucial for timely hormone replacement in patients receiving immunotherapy.
Area of Science:
- Endocrinology
- Oncology
- Immunology
Background:
- Combined immune checkpoint inhibitors (nivolumab-ipilimumab) are used for metastatic melanoma.
- Hypophysitis is a known side effect of immunotherapy, potentially affecting pituitary hormone production.
Observation:
- A patient developed refractory hypokalemia and was diagnosed with ACTH-dependent hypercortisolism 11 weeks after starting immunotherapy.
- Further investigations revealed central hypothyroidism and hypogonadotropic hypogonadism.
- Imaging showed normal adrenal glands and pituitary.
Findings:
- The patient experienced transient central hypercortisolism, indicated by rising cortisol and ACTH levels.
- Cortisol and ACTH levels subsequently decreased, leading to secondary adrenal insufficiency.
- Hormone replacement therapy with levothyroxine and hydrocortisone was initiated.
Implications:
- This case highlights immunotherapy-related hypophysitis with a distinct transient hypercortisolism phase.
- Early recognition of hypercortisolism and its rapid progression to adrenal insufficiency is vital.
- Vigilant laboratory monitoring and timely hormonal replacement are essential to prevent complications in patients on immunotherapy.
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