Pituitary Essentials - The Master Controller

- Anterior Lobe (Adenohypophysis)
- Hormones: 📌 FLAT PiG: FSH, LH, ACTH, TSH, Prolactin, ignore, GH.
- Regulated by hypothalamic releasing/inhibiting hormones.
- Posterior Lobe (Neurohypophysis)
- Stores & secretes: Vasopressin (ADH) & Oxytocin.
- Pituitary Adenomas
- Most common cause of pituitary hormone excess/deficiency.
- Microadenoma (< 1 cm) vs. Macroadenoma (≥ 1 cm).
- Mass effect (macroadenomas): Bitemporal hemianopsia, headache.
⭐ Prolactinomas are the most common pituitary adenoma. Excess prolactin suppresses GnRH, leading to ↓FSH & ↓LH, causing amenorrhea, galactorrhea, and infertility.
Anterior Hyperpituitarism - Gland Overdrive
- Etiology: Primarily caused by pituitary adenomas. Classified by size: microadenomas (<10 mm) or macroadenomas (≥10 mm).
- Syndromes by Hormone Excess:
- Prolactinoma (Most Common): ↑Prolactin.
- Females: Galactorrhea, amenorrhea, infertility.
- Males: ↓Libido, erectile dysfunction, gynecomastia.
- Treatment: Dopamine agonists (e.g., Cabergoline).
- Somatotroph Adenoma: ↑Growth Hormone (GH).
- Children: Gigantism (pre-epiphyseal closure).
- Adults: Acromegaly (coarse facial features, large hands/feet, glucose intolerance).
- Corticotroph Adenoma: ↑ACTH, causing Cushing's Disease.
- Prolactinoma (Most Common): ↑Prolactin.

⭐ Diagnosis of Acromegaly: The best initial test is measuring IGF-1 levels. The most specific diagnostic test is the failure to suppress serum GH following an oral glucose tolerance test (OGTT).
Anterior Hypopituitarism - Running on Empty
- Etiology: Most commonly due to non-functioning pituitary adenomas. Other causes include Sheehan syndrome (postpartum necrosis), apoplexy (hemorrhage/infarction), iatrogenic (surgery, radiation), and infiltrative diseases (e.g., sarcoidosis, hemochromatosis).
- Clinical Presentation: Varies with deficient hormones. Order of loss is often predictable.
- GH: Fatigue, weakness, ↑fat mass (often first sign in adults).
- LH/FSH: ↓ Libido, amenorrhea/erectile dysfunction, infertility.
- TSH: Secondary hypothyroidism (fatigue, cold intolerance).
- ACTH: Secondary adrenal insufficiency (weakness, hypotension).
- 📌 Mnemonic for order of loss: "Go Look For The Adenoma" (GH, LH/FSH, TSH, ACTH).
- Diagnosis: Low basal hormone levels (e.g., 8 AM cortisol, TSH, free T4) plus stimulation tests (e.g., ACTH stimulation test). Pituitary MRI to identify the cause.
⭐ In secondary adrenal insufficiency from hypopituitarism, hyperpigmentation is absent because ACTH and MSH levels are low. Aldosterone secretion is preserved (RAAS control).

Posterior Pituitary - Water Woes
- Antidiuretic Hormone (ADH/Vasopressin): Regulates plasma osmolality by controlling renal water reabsorption. Imbalance leads to Diabetes Insipidus (DI) or SIADH.
| Feature | Central DI | Nephrogenic DI | SIADH |
|---|---|---|---|
| ADH Level | ↓ Low | Normal / ↑ High | ↑ High (inappropriate) |
| Serum Osm | >295 mOsm/kg | >295 mOsm/kg | <275 mOsm/kg |
| Urine Osm | < Serum Osm | < Serum Osm | > Serum Osm |
| Urine Na+ | Variable | Variable | >40 mEq/L |
| Treatment | Desmopressin | Thiazides, NSAIDs | Fluid restriction, Vaptans |
⭐ Ectopic ADH production, most commonly from Small Cell Lung Cancer, is a classic cause of SIADH. Always consider malignancy in a patient with unexplained hyponatremia and concentrated urine.
High‑Yield Points - ⚡ Biggest Takeaways
- Prolactinoma, the most common pituitary tumor, causes galactorrhea; treat with dopamine agonists.
- For acromegaly, the best initial test is IGF-1; a glucose suppression test confirms the diagnosis.
- Cushing's disease is an ACTH-secreting adenoma suppressible by high-dose dexamethasone.
- Sheehan syndrome is postpartum pituitary necrosis causing failure to lactate.
- Central DI responds to desmopressin; nephrogenic DI does not.
- SIADH causes euvolemic hyponatremia; treat with fluid restriction.
- Pituitary adenomas cause bitemporal hemianopsia via optic chiasm compression.
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