Hyperprolactinaemia
Hyperprolactinaemia is a raised serum prolactin level causing galactorrhoea and gondadal dysfunction.
Most common endocrine abnormality of the hypothalamic–pituitary axis.
Prolactin (PRL) is under the inhibitory control of dopamine released from the hypothalamus. Causes of hyperprolactinaemia are shown in Fig. 11.4 and Table 11.4.
Hyperprolactinaemia causes disturbance of the hypothalamic–pituitary–gonadal axis in both men and women, probably by a local hormonal interaction between prolactin and hypothalamic gonadotrophinreleasing hormone (GnRH) secretion.
· Gonadotrophin (luteinising hormone and follicle stimulating hormone (LH and FSH) secretion is abnormal and the midcycle surge in LH in women is suppressed.
· Hyperprolactinaemia in women is commonly physiological, and in men it is almost always of pathological significance.
In women hyperprolactinaemia causes primary or secondary amenorrhoea, oligomenorrhoea with anovulation or infertility. Galactorrhoea is variably present. Oestrogen deficiency can cause vaginal dryness and osteopenia. Hirsutism can occur, with weight gain and anxiety depression and hot flushes. In men galactorrhoea occurs occasionally, but the most common early features are decreased libido and sexual dysfunction, sometimes with impotence and infertility.
Headache, visual impairment and hypopituitarism due to local effects of the adenoma.
Raised PRL in the absence of another cause of hyper-prolactinaemia is the feature of a functioning pituitary adenoma. The serum prolactin level is in proportion to tumour size. All the pituitary hormone axes have to be tested to look for associated hypopituitarism. Plain skull X-ray is usually normal, whereas MRI will demonstrate the lesion, usually <1 cm in size.
Prolactinomas are treated with dopaminergic drugs such as cabergoline. The minority of tumours that do not respond to medical treatment and hyperprolactinaemia due to stalk compression are treated surgically.
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