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A Case of Pituitary Apoplexy Following Leuprolide Injection for Prostate Cancer
Kang Woo Kim1, Sora Chee2, Naveena Sunkara2
1Alpert Medical School of Brown University, Providence, RI.
Pituitary apoplexy is a rare complication of androgen deprivation therapy for prostate cancer. Early recognition and prompt management are crucial for patients receiving GnRH agonist therapy.
Area of Science:
- Endocrinology
- Oncology
- Neurology
Background:
- Androgen deprivation therapy (ADT) using gonadotropin-releasing hormone (GnRH) agonists is a standard treatment for advanced prostate cancer.
- While effective, ADT can rarely lead to serious complications.
- Pituitary apoplexy, a sudden hemorrhage or infarction of the pituitary gland, is a critical but infrequent adverse event associated with this therapy.
Observation:
- A 70-year-old male with prostate cancer developed pituitary apoplexy after initiating leuprolide acetate, a GnRH agonist.
- Symptoms included hot flashes, nausea, vomiting, and cranial nerve III palsy.
- Imaging confirmed a pituitary adenoma with hemorrhage.
Findings:
- The patient was managed conservatively with a multidisciplinary approach.
- Symptoms showed improvement with conservative management.
- This case underscores the potential for GnRH agonist-induced pituitary apoplexy.
Implications:
- Clinicians must maintain a high index of suspicion for pituitary apoplexy in patients on GnRH agonist therapy.
- Prompt investigation of new neuro-ophthalmic symptoms is essential.
- Timely diagnosis and treatment are vital to reduce morbidity in prostate cancer patients undergoing ADT.
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