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Pituitary disorders

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Pituitary Anatomy - Command Center

  • Location: Protected within the sella turcica of the sphenoid bone.
  • Lobes & Embryology:
    • Anterior (Adenohypophysis): From oral ectoderm (Rathke's pouch).
    • Posterior (Neurohypophysis): From neuroectoderm.
  • Anterior Pituitary Hormones: 📌 FLAT PEG
    • Tropic: FSH, LH, ACTH, TSH
    • Direct: Prolactin, Endorphins, GH

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⭐ Pituitary adenomas can compress the optic chiasm superiorly, causing classic bitemporal hemianopsia.

Pituitary Adenomas - Hyperactive Hormones

  • Prolactinoma (Most Common):

    • Secretes ↑ Prolactin → Galactorrhea & amenorrhea (females), ↓ libido & infertility (males).
    • Dx: ↑ serum prolactin.
    • Rx: Dopamine agonists (e.g., Cabergoline, Bromocriptine).
  • Somatotroph Adenoma (↑ GH):

    • Acromegaly (Adults): Large hands/feet, coarse facial features, insulin resistance.
    • Gigantism (Children): ↑ linear growth before epiphyseal closure.
    • Dx: ↑ IGF-1; failure of GH suppression with oral glucose tolerance test.
  • Corticotroph Adenoma (↑ ACTH):

    • Cushing's Disease: The specific cause of Cushing's syndrome due to a pituitary adenoma.
    • Dx: ↑ 24-hr urine free cortisol; failure of low-dose dexamethasone suppression.

⭐ Nelson Syndrome: Post-bilateral adrenalectomy, a pre-existing corticotroph adenoma grows rapidly. Presents with mass effects and hyperpigmentation (↑ MSH).

Acromegaly: Signs and Symptoms

Posterior Pituitary - Wet or Dry

  • SIADH (Wet - ↑ ADH): Euvolemic hyponatremia.

    • Causes: Ectopic (Small cell lung cancer), CNS trauma, drugs.
    • Labs: ↓ Serum Osm, ↑ Urine Osm (>100 mOsm/kg), ↑ Urine Na+ (>40 mEq/L).
    • 📌 Small cell, Increased ADH, Dilutional Hyponatremia.
  • Diabetes Insipidus (Dry - ↓ ADH effect): Hypernatremia & polyuria.

    • Central: ↓ ADH production. Responds to desmopressin.
    • Nephrogenic: Renal ADH resistance. No response.

⭐ Correcting hyponatremia from SIADH too rapidly (>8-12 mEq/L/24h) risks osmotic demyelination syndrome (central pontine myelinolysis).

Hypopituitarism - Powering Down

  • Etiology: Pituitary adenomas (most common), Sheehan syndrome (postpartum necrosis), apoplexy, empty sella syndrome, craniopharyngioma.
  • Clinical Presentation: Sequential loss of hormones.
    • ↓GH → Dwarfism (children)
    • ↓FSH/LH → Amenorrhea, ↓libido
    • ↓TSH → Secondary hypothyroidism
    • ↓ACTH → ↓cortisol, no hyperpigmentation
  • 📌 Sequence of Loss: Go Look For The Adenoma (GH, LH, FSH, TSH, ACTH)

Sheehan Syndrome Pathophysiology

⭐ In pituitary-dependent adrenal insufficiency (↓ACTH), aldosterone levels are preserved by the renin-angiotensin system, but cortisol is low.

Craniopharyngioma - Rathke's Revenge

  • Benign suprasellar tumor from Rathke's pouch remnants (ectoderm).
  • Bimodal age distribution: common in children (5-15 yrs) & adults (>50 yrs).
  • Presents with headaches, visual defects (bitemporal hemianopsia), and panhypopituitarism.
  • Histology: "Wet" keratin, dystrophic calcification, and cysts with "machine oil" fluid (cholesterol crystals).

⭐ Most common childhood supratentorial tumor.

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High‑Yield Points - ⚡ Biggest Takeaways

  • Pituitary adenomas are the most common cause of hyperpituitarism; prolactinomas are the most frequent type.
  • Mass effect from adenomas classically causes bitemporal hemianopsia by compressing the optic chiasm.
  • Sheehan syndrome is postpartum pituitary necrosis, leading to hypopituitarism and failure to lactate.
  • Central Diabetes Insipidus (↓ ADH) causes polyuria and hypernatremia; it responds to desmopressin.
  • SIADH (↑ ADH) results in euvolemic hyponatremia and inappropriately concentrated urine.
  • Pituitary apoplexy, an acute hemorrhage into an adenoma, is a neurosurgical emergency.

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