Pituitary Basics - Master Gland Overview

- Location: Sella turcica, sphenoid bone; connected to hypothalamus by infundibulum (stalk).
- Lobes & Hormones:
- Anterior (Adenohypophysis): GH, PRL, ACTH, TSH, FSH, LH. 📌 Mnemonic: FLAT PiG (FSH, LH, ACTH, TSH, PRL, GH).
- Posterior (Neurohypophysis): Stores & releases ADH (Vasopressin), Oxytocin (from hypothalamus).
- Regulation: Hypothalamic releasing/inhibiting factors (anterior); neural input (posterior).
⭐ The anterior pituitary develops from Rathke's pouch (oral ectoderm); posterior from neuroectoderm (diencephalon).
Anterior Hyperdrive - Excess Hormone Express
Pituitary adenomas causing hormone overproduction.
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Prolactinoma (Most Common)
- Symptoms: Galactorrhea, amenorrhea, infertility, ↓libido.
- Diagnosis: ↑Serum PRL. PRL > 200 ng/mL suggestive. MRI.
- Treatment: Dopamine agonists (Cabergoline > Bromocriptine). Surgery if failure/compression.
-
Acromegaly / Gigantism (GH Excess)
- Gigantism (kids), Acromegaly (adults).
- Symptoms: Coarse facies, large hands/feet, prognathism, arthralgia, HTN, DM.
- Diagnosis: ↑IGF-1 (screen). OGTT: GH not suppressed < $\mathbf{1}$ ng/mL (confirm). MRI.
- Treatment: Transsphenoidal surgery (1st line). Medical: Somatostatin analogs (Octreotide), Pegvisomant.
-
Cushing's Disease (ACTH-secreting adenoma)
- Symptoms: Central obesity, moon facies, buffalo hump, purple striae, HTN, hyperglycemia, osteoporosis.
- Diagnosis: ↑ACTH. Low-dose dexamethasone: no suppression; high-dose: suppression. MRI.
- Treatment: Transsphenoidal surgery (1st line). Medical: Ketoconazole, Metyrapone.

⭐ Prolactinomas are the most common hormone-secreting pituitary tumors.
Anterior Low & Slow - Deficits & Pressure Cookers
- Hypopituitarism (Deficits): ↓Anterior pituitary hormones.
- Causes: Adenomas, Sheehan's, apoplexy, iatrogenic (surgery/XRT).
- 📌 Order of loss: GH → LH/FSH → TSH → ACTH → PRL ("Go Look For The Adenoma").
- Clinical Features:
- GH↓: Child: dwarfism; Adult: ↓muscle, ↑fat, ↓QoL.
- LH/FSH↓: Hypogonadism (amenorrhea, infertility, ↓libido).
- TSH↓: Secondary hypothyroidism (fatigue, cold).
- ACTH↓: Secondary adrenal insufficiency (weakness, hypotension; NO hyperpigmentation/hyperkalemia).
- PRL↓: Lactation failure.
- Pressure Cookers (Tumor Mass Effects): Expanding pituitary lesions.
- Headache: Often bitemporal.
- Visual: Bitemporal hemianopia (optic chiasm).

- CN Palsies: CN III, IV, V1/2, VI palsies (cavernous sinus).
- Pituitary Apoplexy: Acute tumor bleed/infarct. Severe HA, vision loss, ophthalmoplegia, ↓LOC. Emergency!
- Sheehan's Syndrome: Postpartum necrosis. Lactation failure, amenorrhea, hypopituitarism.
⭐ ACTH deficiency: Aldosterone (RAAS) normal → NO hyperkalemia. Low ACTH/MSH → NO hyperpigmentation.
Posterior Pituitary - Water Works Wonders (or Woes)
ADH (Vasopressin) from posterior pituitary controls water balance.
- Diabetes Insipidus (DI): 📌 "Dry Inside" - ↓ADH effect.
- Symptoms: Polyuria (>3L/day), polydipsia, nocturia.
- Labs: ↑Serum Osm (>295 mOsm/kg), ↓Urine Osm (<300 mOsm/kg), ↓Urine Sp. Gr. (<1.005).
- Types:
- Central (↓ADH): Rx Desmopressin. Dx: Water deprivation test + ADH.
- Nephrogenic (Kidney ADH resistance): Rx Thiazides, Amiloride (Li-induced).
- SIADH: 📌 "Soaked Inside" - ↑ADH effect.
- Symptoms: Related to hyponatremia (Na <135 mEq/L); euvolemic.
- Labs: ↓Serum Osm (<275 mOsm/kg), ↑Urine Osm (>100 mOsm/kg), ↑Urine Na (>20 mEq/L).
- Rx: Fluid restriction (<800mL/day), hypertonic saline (severe), Vaptans.
⭐ Ectopic ADH from Small Cell Lung Cancer is a classic cause of SIADH.

High‑Yield Points - ⚡ Biggest Takeaways
- Prolactinoma: Most common functional pituitary adenoma; treat with dopamine agonists (cabergoline).
- Acromegaly/Gigantism: Screen with IGF-1; confirm with OGTT (failed GH suppression).
- Cushing's Disease: ACTH-secreting pituitary adenoma; leads to bilateral adrenal hyperplasia.
- Central Diabetes Insipidus: ↓ADH secretion; water deprivation test confirms; responds to desmopressin.
- SIADH: Characterized by euvolemic hyponatremia; primary treatment is fluid restriction.
- Sheehan's Syndrome: Postpartum pituitary ischemic necrosis causing panhypopituitarism.
- Craniopharyngioma: Suprasellar calcified cystic tumor (Rathke's pouch remnant); visual field defects_._
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