Pituitary tumours
Adenoma of the pituitary (functioning or non-functioning) ± mass effect
Overview
Pituitary adenomas — functioning (prolactinoma, GH→acromegaly, ACTH→Cushing's disease, rarely TSH) or non-functioning. They present through hormone excess, hormone deficiency (compression of normal gland) or mass effect (bitemporal hemianopia from optic chiasm compression, headache, cavernous sinus involvement). Pituitary apoplexy is the acute haemorrhage/infarction.
Recognise
- Mass effect: BITEMPORAL HEMIANOPIA (optic chiasm), headache, cranial-nerve palsies (cavernous sinus), hypopituitarism
- Functioning syndromes: galactorrhoea/amenorrhoea (prolactin), acromegaly (GH), Cushing's disease (ACTH)
- Pituitary apoplexy: sudden severe headache, visual loss, ophthalmoplegia, collapse
Red flags
- Pituitary apoplexy → emergency (steroids + neurosurgery)
- Progressive visual field loss → urgent surgical decompression
Differentials & how to tell them apart
Investigations
MRI pituitary; visual fields/acuity; full pituitary hormone profile (excess and deficiency); prolactin (and beware the hook effect).
Management
Prolactinoma → dopamine agonist; others → transsphenoidal surgery
- 1Characterise function (excess/deficiency) and mass effect (fields, MRI). PROLACTINOMAS are treated medically (dopamine agonist); other functioning/compressive tumours are surgical.Gate: Confirm it is not a prolactinoma before operating — a very high prolactin means dopamine agonist (medical) first, whereas a mild rise with a big tumour is stalk compression needing surgery; apoplexy needs urgent steroids + neurosurgery
- 2Transsphenoidal surgery ± radiotherapy; replace deficient axes; lifelong endocrine and imaging follow-up.
Key points
Bitemporal hemianopia + a sellar mass = pituitary tumour. The single most useful triage: very high prolactin (→ medical) vs everything else (→ surgery). Apoplexy is the emergency.
Monitor & prognosis
Fields, MRI, pituitary axes.
Good; depends on type/size.
Source: Society for Endocrinology; neurosurgery guidance