Almost always benign
< 1cm in diameter = "Microadenomas"
I. Prolactin-secreting tumors (60% of functioning pituitary tumors)
- Clinical features
- Galactorrhea (only in about 1/3)
- Headache
- Diplopia or hemianopsia
- Amenorrhea & infertility
- In men can cause Erectile Dysfunction, decreased libido, and infertility
- Initial evaluation--Coned-down lateral XR of sella turcica is sufficient if PRL is < 100ng/ml and no visual change or HA; otherwise, MRI
- Treatment
- Dopamine agonists (80-90% of microadenomas and 60-75% of macroadenomas will respond)
- Bromocriptine
- Cabergoline (see Med. Lett. 39:58, 1997)
- Long-acting Depot dopamine agonists
- Surgery
- Somatostatin-receptor-subtype-selective analogs
- If no HA or vis. sx, can just check yearly PRL levels & visual field and MRI q2-3y
II. Growth-Hormone secreting tumors (20% of functional pituitary tumors)
- Clinical features
- Acromegaly (us. only after 10y or so)
- Headaches
- Hypopituitarism
- Diplopia or hemianopsia
- Treatment
- Surgery is generally tx of choice
- Somatostatin analogs (e.g. octreotide), sometimes in combination w/bromocriptine
- Somatostatin-receptor-subtype-selective analogs
- GHRH antagonists
- Irradiation
III. ACTH-secreting tumors (15% of functional pituitary tumors)
- Treatment
- Surgery generally tx of choice but may result in hypocortisolism
- Irradiation + Cortisol-decreasing drugs (e.g. mitotane, ketaconazole, aminoglutethimide, and metapyrone)
IV. TSH-secreting tumors--RARE
- Treatment
- Surgery + irradiation are generally tx of choice
- Somatostatin analogs, e.g. octreotide
V. Nonfunctioning tumors (1/3 of all pituitary tumors; the most common macroadenomas)
- Clinical presentation
- Headache
- Diplopia or hemianopsia
- Hypopituitarism
- Hypogonadism, occasionally
- Treatment
- Surgery is generally tx of choice
- Irradiation
- GRH antagonists
(Source: summary of Ann. Int. Med. 129:472, 1998--AFP)