What is the inpatient endocrine workup for a suprasellar (located above the sella turcica) mass?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: August 8, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Inpatient Endocrine Workup for Suprasellar Mass

The comprehensive inpatient endocrine workup for a suprasellar mass should include morning pituitary hormone testing (TSH, free T4, ACTH, cortisol, gonadal hormones), followed by high-resolution MRI of the sella with contrast as the primary imaging modality. 1

Initial Hormonal Evaluation

Baseline Pituitary Function Assessment

  • Morning hormone panel (preferably around 8 AM):
    • Thyroid function: TSH and free T4 (to assess for central hypothyroidism) 1
    • Adrenal function: ACTH and cortisol (to assess for central adrenal insufficiency) 1
    • Gonadal function:
      • Males: Testosterone, FSH, LH
      • Females: Estradiol, FSH, LH 1
    • Growth hormone axis: IGF-1 (as a surrogate for GH function)
    • Prolactin: To assess for hyperprolactinemia (which may be from the mass itself or from stalk effect)

Additional Endocrine Testing

  • 1 mcg cosyntropin stimulation test: If morning cortisol is borderline or if there is high clinical suspicion for adrenal insufficiency 1
  • Glucose monitoring: Fasting glucose and HbA1c to assess for diabetes insipidus or other glycemic abnormalities 1
  • Water deprivation test: If diabetes insipidus is suspected based on polyuria and hypernatremia

Imaging Studies

Primary Imaging

  • MRI sella with high-resolution pituitary protocol: The preferred diagnostic imaging modality 1
    • Should include both pre-contrast and post-contrast sequences
    • Thin-section, focused field-of-view sequences targeted for sellar and parasellar assessment
    • Allows characterization of the mass and its relationship to surrounding structures (optic chiasm, cavernous sinus, etc.)

Complementary Imaging

  • CT sella: May provide complementary information about bony anatomy and calcifications 1
    • Particularly useful for surgical planning
    • Less sensitive than MRI for soft tissue characterization

Clinical Considerations

Urgent Assessment for Adrenal Insufficiency

  • Central adrenal insufficiency is a potentially life-threatening complication of suprasellar masses
  • If suspected, initiate stress-dose glucocorticoids before confirmatory testing is complete
  • Monitor for signs of adrenal crisis: hypotension, hyponatremia, hyperkalemia, hypoglycemia 1, 2

Visual Field Assessment

  • Formal visual field testing should be performed due to the proximity of the optic chiasm
  • Document any visual deficits as baseline before treatment

Management Considerations

Perioperative Hormone Replacement

  • Glucocorticoid replacement: Required in all patients with evidence of adrenal insufficiency 2
    • Hydrocortisone 2 mg/kg at induction
    • Continue IV hydrocortisone until oral intake is resumed
  • Thyroid hormone replacement: For patients with central hypothyroidism
    • Only start after adequate glucocorticoid coverage to avoid precipitating adrenal crisis 1

Common Pitfalls to Avoid

  • Failure to diagnose adrenal insufficiency: Can lead to life-threatening adrenal crisis during surgery or other stressful events
  • Premature thyroid hormone replacement: Starting levothyroxine before glucocorticoid replacement in patients with both deficiencies can precipitate adrenal crisis
  • Misdiagnosis of reversible causes: Some suprasellar masses (like those secondary to primary hypothyroidism) may resolve with appropriate hormone replacement 3
  • Missing late endocrine complications: Even after successful treatment of the mass, patients may develop delayed endocrine abnormalities requiring long-term follow-up 4

Differential Diagnosis Considerations

Different suprasellar masses have distinct endocrine profiles that can help guide diagnosis:

  • Pituitary adenoma with suprasellar extension: Often presents with specific hormone excess or deficiency
  • Craniopharyngioma: Typically presents with multiple anterior pituitary hormone deficiencies
  • Rathke's cleft cyst: May cause variable hormone deficiencies
  • Meningioma: Often presents with gradual onset of hypopituitarism
  • Hypothalamic glioma: May present with diabetes insipidus and growth failure 5

The endocrine workup, combined with imaging characteristics, helps differentiate between these entities and guides appropriate management.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Adrenal Nodule Management

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Research

Long-term endocrine outcome of suprasellar arachnoid cysts.

Journal of neurosurgery. Pediatrics, 2017

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.