Skip to content
2000
Volume 20, Issue 3
  • ISSN: 1871-5303
  • E-ISSN: 2212-3873

Abstract

Introduction: Adrenocortical carcinoma (ACC) is a rare neoplasm characterized by a high risk of recurrence after radical resection. The role of adjuvant systemic therapy in radically resected patients is unclear. Mitotane, a steroidogenesis inhibitor, is the only drug approved for the systemic treatment of advanced ACC. In 2007, a retrospective case-control study provided the evidence that mitotane, administered for two years after successful surgery, could prolong recurrence-free survival. Adrenal insufficiency (AI), which occurs in almost all patients during the first 12 months of treatment, is an expected side effect of mitotane and requires steroid replacement therapy. Due to its long halflife, mitotane-induced AI persists several months after treatment discontinuation and is managed by cautious tapering of glucocorticoid replacement therapy. Results: We report a case of symptomatic AI diagnosed after a severe allergic reaction occurring three years after the discontinuation of adjuvant mitotane therapy. Conclusion: The case suggests that mitotane-induced AI should be monitored for a long time to asses full recovery of adrenal function, in order to prevent adrenal crises.

Loading

Article metrics loading...

/content/journals/emiddt/10.2174/1871530319666190809144620
2020-04-01
2025-05-23
Loading full text...

Full text loading...

/content/journals/emiddt/10.2174/1871530319666190809144620
Loading

  • Article Type:
    Case Report
Keyword(s): adjuvant; Adrenal cancer; adrenal insufficiency; mitotane; pharmacology; treatment
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error
Please enter a valid_number test