Related Subjects:
|Adrenal Physiology
|Addisons Disease
|Phaeochromocytoma
|Adrenal Adenomas
|Adrenal Cancer
|Cushing Syndrome
|Cushing Disease
|Congenital Adrenal hyperplasia
|Primary hyperaldosteronism (Conn's syndrome)
|ACTH
|McCune Albright syndrome
|Male Infertility
|Prolactin
|Prolactinoma
|Sheehan's syndrome
⚠️ Always give stress-dose steroids (at least double maintenance) during illness, infection, trauma, or surgery.
💡 In suspected but undiagnosed hypopituitarism, administer steroids before pursuing investigations — cortisol replacement is lifesaving.
📖 About
- The anterior pituitary releases six key hormones 🧬:
LH, FSH, GH, TSH, ACTH, Prolactin.
🧬 Causes of Hypopituitarism
- 🎭 Pituitary adenoma (non-functioning or hormone-secreting e.g. prolactinoma).
- 👶 Craniopharyngioma – common in children.
- 🌿 Infiltrative diseases: sarcoidosis, TB, haemochromatosis.
- 💉 Vascular: Sheehan’s syndrome (postpartum), pituitary apoplexy (acute infarction/bleed).
- 🦠 Infectious: meningitis, encephalitis, syphilis.
- 🤕 Trauma: esp. basal skull fractures.
- 🧬 Congenital: Kallmann syndrome (GnRH deficiency + anosmia).
- 🛡️ Autoimmune: anti-pituitary antibodies.
- ⚡ Other: anorexia, starvation, radiotherapy, chemotherapy.
🩺 Clinical Presentation
- ACTH deficiency 🧪: low cortisol → fatigue, hypotension. Mineralocorticoids preserved (distinguishes from Addison’s).
- Prolactin deficiency 🍼: impaired lactation; ↑ prolactin may signal stalk compression (“stalk effect”).
- LH & FSH deficiency ❤️: infertility, ↓ libido, amenorrhoea/impotence.
- GH deficiency 📏: children – short stature; adults – ↓ muscle bulk, energy.
- TSH deficiency 🌀: central hypothyroidism.
- ADH deficiency 💧: diabetes insipidus if posterior pituitary involved.
👁️ Local Effects of Pituitary Lesions
- Headache.
- Bitemporal hemianopia 👓 (optic chiasm compression).
- Cranial nerve palsies (III, IV, VI) if cavernous sinus involved.
- Pituitary hormone deficiencies.
🔍 Investigations
- Hormone profile: prolactin, TSH + T4, 9am cortisol, IGF-1, GH, FSH, LH, oestrogen/testosterone.
- Metabolic profile: fasting glucose, HbA1c.
- 🧲 MRI pituitary (gold standard for mass lesions).
💊 Management
- Acute hypopituitarism 🚨: IV hydrocortisone 100 mg q6h immediately.
- Hydrocortisone replacement 💉: oral 15–40 mg/day (e.g. 15 mg AM, 5 mg PM).
- Thyroid replacement 🌀: L-thyroxine titrated to normal T4 (not TSH, as central disease).
- Gonadal hormones ❤️:
- Males: testosterone (IM/oral/gel/implant) if fertility not required; gonadotropins if fertility desired.
- Females: oestrogen-progesterone if fertility not required; gonadotropins or pulsatile GnRH if fertility required.
- Growth hormone 📏: consider in children; in adults rarely used (possible malignancy risk).
📚 Exam Tip:
- In acute hypopituitarism, give steroids first.
- Central hypothyroidism → monitor with T4 (not TSH).
- ACTH deficiency spares mineralocorticoids (unlike Addison’s).
Cases — Hypopituitarism (Pituitary Failure)
- Case 1 — Pituitary adenoma 🧠: A 48-year-old man presents with fatigue, erectile dysfunction, and reduced libido. Exam: bitemporal hemianopia. Bloods: low testosterone, low LH/FSH, low cortisol, low T4 with inappropriately normal TSH. MRI: large pituitary macroadenoma compressing the optic chiasm. Diagnosis: hypopituitarism secondary to pituitary adenoma. Managed with hormone replacement (hydrocortisone, thyroxine, testosterone) and trans-sphenoidal surgery.
- Case 2 — Sheehan’s syndrome 🩸: A 32-year-old woman presents 3 months after a postpartum haemorrhage with failure to lactate, secondary amenorrhoea, fatigue, and weight loss. Bloods: low prolactin, low gonadotropins, low cortisol, low T4. Diagnosis: postpartum pituitary necrosis (Sheehan’s syndrome). Managed with lifelong hormone replacement (hydrocortisone, thyroxine, oestrogen/progesterone replacement).
- Case 3 — Radiotherapy-induced ⚡: A 55-year-old man treated with cranial radiotherapy for nasopharyngeal carcinoma 10 years ago presents with progressive fatigue, cold intolerance, and reduced exercise tolerance. Bloods: low IGF-1, low cortisol, low T4, low gonadotropins. Diagnosis: panhypopituitarism secondary to radiotherapy. Managed with staged hormone replacement (hydrocortisone before thyroxine, then sex steroids, GH if appropriate).
Teaching Point 🩺: Hypopituitarism = partial or complete deficiency of pituitary hormones.
Common causes: pituitary adenoma, surgery, radiotherapy, infarction (Sheehan’s), trauma, infiltrative disease.
Clinical features depend on which hormones are deficient:
- ACTH: fatigue, adrenal crisis.
- TSH: hypothyroidism.
- LH/FSH: infertility, amenorrhoea, low libido.
- GH: reduced muscle mass, increased fat, low energy.
- Prolactin: failure to lactate.
Always replace hydrocortisone before thyroxine to avoid adrenal crisis.