Workup and Treatment of Pituitary Adenomas
Pituitary adenomas require a comprehensive multidisciplinary approach with transsphenoidal surgery as the first-line treatment for most adenomas except prolactinomas, which are primarily treated with dopamine agonists like cabergoline. 1, 2, 3
Initial Diagnostic Workup
Imaging
- MRI of the pituitary gland:
- Pre-contrast T1-weighted and T2-weighted sequences
- Post-contrast with gadolinium enhancement (macrocyclic agents preferred)
- 3-Tesla MRI if available for better resolution 1
Visual Assessment
- Visual acuity testing (logarithm of the minimum angle of resolution)
- Visual field testing (Goldmann perimetry preferred)
- Fundoscopy
- Consider optical coherence tomography for baseline assessment if severe deficits 1
Hormonal Evaluation
- Complete hormonal panel:
Additional Testing
- For suspected Cushing's disease: Consider bilateral inferior petrosal sinus sampling (BIPSS) 4
- Genetic testing if:
- Family history of pituitary adenomas
- Young age at presentation
- Multiple endocrine neoplasia suspicion
- Consider screening for MEN1, AIP, CABLES1, CDKN1B, and DICER1 mutations 1
Classification of Pituitary Adenomas
By Size
By Function
- Functioning adenomas (hormone-secreting):
- Prolactinomas (32-66%)
- Growth hormone-secreting (8-16%)
- ACTH-secreting (2-6%)
- TSH-secreting (1%)
- Non-functioning adenomas (15-54%) 2, 3
Treatment Approach
Prolactinomas
- First-line: Medical therapy with dopamine agonists
- Second-line: Consider surgery if:
All Other Functioning Adenomas
- First-line: Transsphenoidal surgery
- Endoscopic approach preferred over microscopic for better preservation of pituitary function 1
- Second-line: Medical therapy based on adenoma type:
Non-functioning Adenomas
- Symptomatic (mass effect, hypopituitarism):
- Asymptomatic incidentalomas:
Radiotherapy
- Indications:
- Incomplete tumor resection
- Recurrence after surgery
- Uncontrolled growth despite medical therapy
- Contraindication to surgery 1
- Options:
- Conventional fractionated radiotherapy
- Stereotactic radiosurgery
- Proton beam therapy 4
Perioperative Management
- Strict fluid and electrolyte monitoring
- Watch for diabetes insipidus, SIADH, or triphasic response
- Monitor for hypopituitarism 1
Long-term Follow-up
- Lifelong monitoring for:
- Tumor recurrence (can occur up to 15 years after treatment)
- Hormonal status
- Development of hypopituitarism
- Visual function if previously affected 4
- After radiotherapy: Periodic assessment of radiation efficacy with temporary withdrawal of medical therapy 1
- Mental health monitoring (especially for Cushing's disease patients) 4
Special Considerations
Pediatric Patients
- Transsphenoidal surgery is safe and effective even with incompletely pneumatized sphenoid sinuses
- Consider transition planning to adult services 1
Genetic Syndromes
- MEN1: Higher risk of prolactinomas and non-functioning adenomas
- AIP mutations: Often associated with GH-secreting tumors
- DICER1: Associated with pituitary blastoma 1
Common Pitfalls to Avoid
Misdiagnosis: Consider differential diagnoses including craniopharyngioma, Rathke's cleft cyst, meningioma, and lymphocytic hypophysitis 4, 7
Inadequate hormonal evaluation: Always assess for both hormone hypersecretion and hypopituitarism 4, 2
Overlooking visual assessment: All macroadenomas require formal visual field testing 1, 4
Insufficient follow-up: Recurrences can occur many years after initial treatment 4
Ignoring mental health: Hormonal imbalances can significantly impact psychological wellbeing 4