Benign neoplasm emerging from the cells of the adrenal cortex
Aetiology
- Found in almost all age groups but increase in frequency with age
Pathophysiology
- Majority (~95%) are non-functioning and asymptomatic
- Well circumscribed, encapsulated lesions
- Solitary, small (2 to 3 cm), bright yellow (lipid) and buried within the gland - do not cause a mass lesion
Histological features
- Composed of cells resembling adrenocortical cells
- Well-differentiated, small nuclei
Clinical presentation
- Often incidental finding during abdominal imaging
- Patients with hyperfunctioning adrenal gland adenomas present with manifestations of excess hormone secretion e.g. Cushing's, Conn syndrome
Investigations
Management
- A small adrenal lesion with typical features of an adenoma and without biochemical abnormality can be safely left in situ
- Surgical excision required if:
- Functioning lesion
- Large lesion (>3-5 cm) as considered potentially malignant