Pituitary Tumours
Pituitary space occupying tumours /lesions
- Mass effects , excess hormone secretion, Hypopituitarism
Infiltration
- Visual field defects (bitemporal hemianopia)
- Cavernous sinus – CN 3/4/6 palsy
- Meninges – headache
- Hydrocephalus – Ventricle interruption
- Rhinorrhoea – sphenoid sinus
Diagnosis
MRI > CT, more sensitiveHormone excess
- Prolactinoma (chromophobe) , acromegaly/gigantism(acidophile) , cushing/nelson (basophil)
- Treatment
- Surgery – trans-sphenoidal, transfrontal (large tumours)
- Radiotherapy – gamma knife
- Medical therapy – somatostatin analogues (octreotide), dopamine agonist
Other tumours
- Craniopharyngioma – cystic calcified tumour from Rathke pouch (children)
- Meningioma, gliomas, primary carcinoma – all very rare
Hyperprolactinemia
- Prolactin promotes milk secretion and inhibits gonadal activity
- Inhibited by dopamine
- Mild increases are physiological (400-600mU/L). Very high mostly likely tumour (>5000mU/L)
Etiology
- Tumour, stalk compression, polycystic ovary syndrome, idiopathic, dopamine antagonist (metoclopramide/domperidone), anti-emetics, renal/liver failure
Clinical features
- Galactorrhoea, oligomenorrhoea, decrease libido, subfertility,
- Osteoporosis – oestrogen/androgen deficiency
- Gyncomastia , visual loss, headaches
Diagnosis
- Serum prolactin, IgG (macroprolactinemia)
- Visual examination
- Primary hypothyroidism, anterior pituitary function
- MRI
- Prolactin >5000mU/L suggests prolactinoma and not due to stalk disconnection
Treatment
- Cabergoline – once a week (may cause lung/cardiac fibrosis)
- Bromocriptine – initial [1mg/day] up to [2.5mg/day]