Hormonal Evaluation in Pituitary Macroadenoma
All patients with pituitary macroadenomas require comprehensive evaluation of all anterior pituitary hormone axes to assess for both hypopituitarism and hormone hypersecretion, as hypopituitarism affects 37-85% of these patients. 1
Essential Hormone Panel
Assessment for Hypopituitarism (Hormone Deficiency)
The Congress of Neurological Surgeons recommends routine endocrine analysis of all anterior pituitary axes, given the extremely high prevalence of hormonal deficiencies in macroadenomas 1:
Growth Hormone (GH) Axis: Measure IGF-1 (insulin-like growth factor 1), as GH deficiency is the most common deficit, occurring in 61-100% of patients 1, 2
Gonadal Axis: Measure testosterone (in men), estradiol (in women), FSH, and LH, as central hypogonadism occurs in 36-96% of patients 1, 2
Adrenal Axis: Measure morning (9 AM) cortisol and ACTH, as adrenal insufficiency occurs in 17-62% of patients 1, 2
Thyroid Axis: Measure TSH and free T4, as central hypothyroidism occurs in 8-81% of patients 1, 2
Assessment for Hormone Hypersecretion
Prolactin: Measure serum prolactin in all patients, as hyperprolactinemia occurs in 25-65% of patients with macroadenomas (mean level 39 ng/mL), even when not clinically suspected 1, 2
IGF-1: This serves dual purpose—assessing both for GH deficiency and for acromegaly (GH hypersecretion) 1, 2
Critical Clinical Context
Why This Comprehensive Approach Matters
The Congress of Neurological Surgeons emphasizes that panhypopituitarism (deficiency of all pituitary hormones) occurs in 6-29% of patients with macroadenomas 1, 2. Missing even one axis can lead to life-threatening complications, particularly undiagnosed adrenal insufficiency.
Pattern Recognition for Interpretation
Central hypothyroidism: Low free T4 with low or inappropriately normal TSH (not elevated as in primary hypothyroidism) 2, 3
Central adrenal insufficiency: Low cortisol with low or inappropriately normal ACTH 2, 3
Hypogonadotropic hypogonadism: Low testosterone/estradiol with low or inappropriately normal FSH and LH 2, 3
Additional Metabolic Assessment
- Glucose and HbA1c: To assess glycemic control, as pituitary disorders frequently affect metabolism 2, 3
Critical Management Pitfall to Avoid
If both adrenal insufficiency and hypothyroidism are present, always initiate corticosteroid replacement before thyroid hormone replacement to avoid precipitating an adrenal crisis. 2, 3 This is a potentially fatal error if the sequence is reversed.
What NOT to Order
The Congress of Neurological Surgeons found no evidence supporting routine biomarker testing (such as alpha-subunit or chromogranin A) or genetic testing in patients with sporadic macroadenomas 1. The exception is in children and young people, where genetic assessment should be offered due to higher prevalence of genetic abnormalities 2.
Timing Considerations
Diabetes insipidus is uncommon at presentation in macroadenomas (only 7% of patients) 1, so posterior pituitary assessment is not routinely required unless polyuria/polydipsia is present.