Wednesday, October 10, 2012

Pituitary Macroadenoma

Approach to Pituitary Macroadenoma


  • Pituitary adenomas are classified based on size and function:
    • Macroadenoma vs Microadenoma
    • Functioning vs non-functioning
  • Causes problems by:
    • Hypersecretion: Most common are gonadotroph secreting adenomas, but they are hardest to recognize as they secrete inefficiently and the effects are not easily noticed; prolactin (PRL), responsible for amenorrhea-galactorrhea in women and decreased libido in men; growth hormone (GH), responsible for acromegaly; adrenocorticotropic hormone (ACTH), responsible for Cushing's disease; thyroid-stinulating hormone (TSH), responsible for hyperthyroidism. 
    • Depressed secretion of hormones: Hypopituitarism, in the order of: GH, LH/FSH, TSH, ACTH, PRL (aka Go Look For The Adenoma Please)
    • Mechanical compression
      • Expansion of dura causes headaches
      • Superior invasion: affects optic chiasm and causes bitemporal hemianopsia
      • Inferior invasion: Through cribriform plate into sphenoid sinus causing CSF rhinorrea and risk of meningitis
      • Lateral invasion: Cavernous sinus/internal carotid artery and cranial nerves 3, 4, 6, 5 (V1/V2)
  • Investigation:
    • Mechanical compression/extension: 
      • Assessed by MRI
      • Also can do visual field testing
    • Hormone secretion:
      • GH: is normally secreted in a diurnal pattern and is suppressed by glucose load. Tested by doing an oral glucose tolerance test. Also can test IGF-1 which does not change hour by hour and reflects integrated GH secretion during the previous 24hrs. Also can test response to OGTT, as patients have insulin resistance.
      • TSH/T3/T4
      • Cortisol: Screening tests: 24 UFC, late night salivary cortisol, 1mg Dex suppression test
      • Prolactin: Prolactin level
    • Hormone suppression:
      • GH, LH/FSH/Testosterone, TSH, AM cortisol, prolactin
    • Comorbidities:
      • If patient found to have GH secreting adenoma should look for visceral organ effects:
        • Colonoscopy to look for polyps/colon ca
        • ECHO to look for cardiomyopathy
        • BP to look for HTN
        • Fasting BG, OGTT to screen for diabetes
        • Screen for obstructive sleep apnea
  • Management:
    • Surgical indications:
      • A visual field deficit due to the lesion or other visual abN
      • Adenoma abutting the optic chiasm on MRI
      • Pituitary apoplexy with visual disturbance
      • Hypersecreting tumour other than prolactinoma
    • Specific situations
      • GH secreting adenoma: First line is surgery. Medical therapies include somatostatin analogues (octreotide/lanreotide) and dopamine agonist (cabergoline) and GH receptor antagonists (Pegvisomant). Can also use radiation (fractionated or by Gamma knife).
      • ACTH secreting tumour: primary therapy is surgery
      • Prolactinoma: Can use medical therapy with DA agonist.
    • Micro-incidentalomas
      • Follow-up MRI in 1 yr and then Q1-2 y thereafter
      • If grows significantly (in proportion to original size) then consider surgery
    • Macro-incidentalomas
      • Follow up MRI in 6 months then Q1yr
      • Evaluate for hypopituitarism and evaluate the visual fields
      • If there is tumour growth, VF abN or hypopit consider surgery

See the Endocrine Society Practice Guidelines for an Approach to Pituitary Incidentaloma

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