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
โ ๏ธ Always give stress-dose steroids (at least double maintenance) during illness, infection, trauma, or surgery.
๐ก In suspected but undiagnosed hypopituitarism, administer steroids before pursuing investigations โ cortisol replacement is lifesaving.
๐ About
- The anterior pituitary releases six key hormones ๐งฌ:
LH, FSH, GH, TSH, ACTH, Prolactin.
๐งฌ Causes of Hypopituitarism
- ๐ญ Pituitary adenoma (non-functioning or hormone-secreting e.g. prolactinoma).
- ๐ถ Craniopharyngioma โ common in children.
- ๐ฟ Infiltrative diseases: sarcoidosis, TB, haemochromatosis.
- ๐ Vascular: Sheehanโs syndrome (postpartum), pituitary apoplexy (acute infarction/bleed).
- ๐ฆ Infectious: meningitis, encephalitis, syphilis.
- ๐ค Trauma: esp. basal skull fractures.
- ๐งฌ Congenital: Kallmann syndrome (GnRH deficiency + anosmia).
- ๐ก๏ธ Autoimmune: anti-pituitary antibodies.
- โก Other: anorexia, starvation, radiotherapy, chemotherapy.
๐ฉบ Clinical Presentation
- ACTH deficiency ๐งช: low cortisol โ fatigue, hypotension. Mineralocorticoids preserved (distinguishes from Addisonโs).
- Prolactin deficiency ๐ผ: impaired lactation; โ prolactin may signal stalk compression (โstalk effectโ).
- LH & FSH deficiency โค๏ธ: infertility, โ libido, amenorrhoea/impotence.
- GH deficiency ๐: children โ short stature; adults โ โ muscle bulk, energy.
- TSH deficiency ๐: central hypothyroidism.
- ADH deficiency ๐ง: diabetes insipidus if posterior pituitary involved.
๐๏ธ Local Effects of Pituitary Lesions
- Headache.
- Bitemporal hemianopia ๐ (optic chiasm compression).
- Cranial nerve palsies (III, IV, VI) if cavernous sinus involved.
- Pituitary hormone deficiencies.
๐ Investigations
- Hormone profile: prolactin, TSH + T4, 9am cortisol, IGF-1, GH, FSH, LH, oestrogen/testosterone.
- Metabolic profile: fasting glucose, HbA1c.
- ๐งฒ MRI pituitary (gold standard for mass lesions).
๐ Management
- Acute hypopituitarism ๐จ: IV hydrocortisone 100 mg q6h immediately.
- Hydrocortisone replacement ๐: oral 15โ40 mg/day (e.g. 15 mg AM, 5 mg PM).
- Thyroid replacement ๐: L-thyroxine titrated to normal T4 (not TSH, as central disease).
- Gonadal hormones โค๏ธ:
- 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 ๐: consider in children; in adults rarely used (possible malignancy risk).
๐ Exam Tip:
- In acute hypopituitarism, give steroids first.
- Central hypothyroidism โ monitor with T4 (not TSH).
- ACTH deficiency spares mineralocorticoids (unlike Addisonโs).
Cases โ Hypopituitarism (Pituitary Failure)
- Case 1 โ Pituitary adenoma ๐ง : 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 โ Sheehanโs syndrome ๐ฉธ: 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 (Sheehanโs syndrome). Managed with lifelong hormone replacement (hydrocortisone, thyroxine, oestrogen/progesterone replacement).
- Case 3 โ Radiotherapy-induced โก: 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 ๐ฉบ: Hypopituitarism = partial or complete deficiency of pituitary hormones.
Common causes: pituitary adenoma, surgery, radiotherapy, infarction (Sheehanโs), 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.