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A Large Benign Adrenocortical Adenoma Cosecreting Testosterone and Cortisol.

Authors :
Dillon, Martha
Shteyman, Sara
Rabiehashemi, Samaneh
Madhavan, Parvathy
Luthra, Pooja
Source :
JCEM Case Reports. May2024, Vol. 2 Issue 5, p1-6. 6p.
Publication Year :
2024

Abstract

Most adrenal incidentalomas are benign neoplasms of the adrenal cortex. While the majority are nonfunctional, many secrete cortisol. Androgen- or estrogen-secreting adenomas are rare. A 44-year-old female, with history of hypertension and prediabetes, presented with worsening acne, hirsutism, secondary amenorrhea for 2 years, and a 40-pound weight gain. Laboratory evaluation showed high 24-hour urine free cortisol, suppressed adrenocorticotropic hormone (ACTH) level, indicative of ACTH independent Cushing syndrome, and elevated testosterone and androstenedione. Abdominal computed tomography (CT) revealed a 6.3 × 5.2 × 5.6 cm left adrenal mass. Patient underwent left open adrenalectomy. Pathology revealed benign adrenocortical adenoma. Postoperatively there was a significant improvement in her blood pressure and blood sugar levels, resumption of menses, and complete resolution of hyperandrogenism and hypercortisolism. We describe a patient with an adrenal adenoma cosecreting cortisol and androgen, leading to Cushing syndrome and significant virilization. Adrenal masses secreting androgens are less common and concerning for adrenocortical carcinoma (ACC). Patients with adrenal masses cosecreting multiple hormones should undergo workup expediently since ACC confers poor outcomes. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
27551520
Volume :
2
Issue :
5
Database :
Academic Search Index
Journal :
JCEM Case Reports
Publication Type :
Academic Journal
Accession number :
177680959
Full Text :
https://doi.org/10.1210/jcemcr/luae045