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09-SEPTEMBER-2008 02:07:44 - Hyperprolactinaemia December 2007 Hyperprolactinemia Classification and external resources ICD-10 E22.1 ICD-9 253.1 DiseasesDB 6314 eMedicine med/1098 MeSH D006966 Hyperprolactinaemia BrE or hyperprolactinemia AmE is the presence of abnormally-high levels of prolactin in the blood. Normal levels are less than 580 mIU/L for women, and less than 450 mIU/L for men. The hormone prolactin is downregulated by dopamine and is upregulated by estrogen. A falsely-high measurement may occur due to the presence of the biologically-inactive macroprolactin in the serum. This can show up as high prolactin in some types of tests, but is asymptomatic. Contents 1 Causes 1.1 Physiological causes 1.2 Prescription drugs 1.3 Diseases 1.4 Idiopathic 2 Symptoms 3 Diagnosis 4 Historical eponyms 5 References Causes Hyperprolactinaemia may be caused by either disinhibition e.g., compression of the pituitary stalk or reduced dopamine levels or excess production from a prolactinoma a pituitary gland adenoma tumour. A blood serum prolactin level of 1000-5000 mIU/L could be from either mechanism, but 5000 mIU/L is likely due to the activity of an adenoma with macroadenomas large tumours over 10 mm diameter whose levels of prolactin are up to 100,000 mIU/L. Hyperprolactinemia inhibits gonadotropin-releasing hormone GnRH by increasing the release of dopamine from the arcuate nucleus of the hypothalamus dopamine inhibits GnRH secretion, thus inhibiting gonadal steroidogenesis, which is the cause of many of the symptoms described below. There is a suspicion that Minoxidil, a potassium channel opener, may be related to the development of this disease. A two-year test with Minoxidil, under normal dosing parameters, was carried out on rats, which caused pheochromocytomas in both males and females, and preputial gland adenomas in males1. Physiological causes Physiological causes i.e., as result of normal body functioning: pregnancy, breastfeeding, stress, sleep. Prescription drugs Use of prescription drugs is the most common cause of hyperprolactinaemia. Prolactin secretion in the pituitary is normally suppressed by the brain chemical dopamine. Drugs that block the effects of dopamine at the pituitary or deplete dopamine stores in the brain may cause the pituitary to secrete prolactin. These drugs include the major tranquilizers phenothiazines, trifluoperazine Stelazine, and haloperidol Haldol; some antipsychotic medications; metoclopramide Reglan, used to treat gastroesophageal reflux and the nausea caused by certain cancer drugs; and, less often, alpha-methyldopa and reserpine, used to control hypertension; and oestrogens and TRH. Diseases Prolactinoma or other tumors arising in or near the pituitary - such as those that cause acromegaly or Cushing's syndrome - may block the flow of dopamine from the brain to the prolactin-secreting cells, likewise, division of the pituitary stalk or hypothalamic disease. Other causes include chronic renal failure, hypothyroidism, and sarcoidosis. Some women with polycystic ovary syndrome may have mildly-elevated prolactin levels. Apart from diagnosing hyperprolactinaemia and hypopituitarism, prolactin levels are often determined by physicians in patients that have suffered a seizure, when there is doubt as to whether this was an epileptic seizure or a non-epileptic seizure. Shortly after epileptic seizures, prolactin levels often rise, whereas they are normal in non-epileptic seizures. Idiopathic In many patients, elevated levels remain unexplained and may represent a form of hypothalamic-pituitary dysregulation. Symptoms In women, a high blood level of prolactin often causes hypoestrogenism with anovulatory infertility and a decrease in menstruation. In some women, menstruation may disappear altogether amenorrhea. In others, menstruation may become irregular or menstrual flow may change. Women that are not pregnant or nursing may begin producing breast milk. Some women may experience a loss of libido interest in sex. Intercourse may become painful because of vaginal dryness. In men, the most common symptoms of hyperprolactinemia are decreased libido, erectile dysfunction, and infertility. Because men have no reliable indicator such as menstruation to signal a problem, many men with hyperprolactinemia being caused by an adenoma may delay going to the doctor until they have headaches or eye problems caused by the enlarged pituitary pressing against nearby optic nerves. They may not recognize a gradual loss of sexual function or libido. Only after treatment do some men realize they had a problem with sexual function. In men excess prolactin may also cause Gynecomastia. Because of hypoestrogenism, hyperprolactinaemia can lead to osteoporosis. Diagnosis A doctor will test for prolactin blood levels in women with unexplained milk secretion galactorrhea or irregular menses or infertility, and in men with impaired sexual function and, in rare cases, milk secretion. If prolactin is high, a doctor will test thyroid function and ask first about other conditions and medications known to raise prolactin secretion. While a plain X-ray of the bones surrounding the pituitary may reveal the presence of a large macro-adenoma, the small micro-adenoma will not be apparent. Magnetic resonance imaging MRI is the most sensitive test for detecting pituitary tumors and determining their size. MRI scans may be repeated periodically to assess tumor progression and the effects of therapy. Computed Tomography CT scan also gives an image of the pituitary, but it is less sensitive than the MRI. In addition to assessing the size of the pituitary tumor, doctors also look for damage to surrounding tissues, and perform tests to assess whether production of other pituitary hormones is normal. Depending on the size of the tumor, the doctor may request an eye exam with measurement of visual fields. Historical eponyms The following eponyms were established before prolactin levels could be measured reliably in the clinical setting. On occasion, they are still encountered: Ahumada-DelCastillo Syndrome, which refers to the association of galactorrhea and amenorrhea Chiari-Frommel Syndrome, which refers to extended postpartum galactorrhea and amenorrhea Forbes-Albright Syndrome, which refers to galactorrhea-amenorrhea associated with a pituitary tumor. References ^ Minoxidil Official FDA information, side effects and uses v d e Endocrine pathology: endocrine diseases E00-35, 240-259 Pancreas/ glucose metabolism Diabetes mellitus types: type 1, type 2, MODY, complications: coma, angiopathy, ketoacidosis, nephropathy, neuropathy, retinopathy Hypoglycemia - Hyperinsulinism - Zollinger-Ellison syndrome - insulin receptor Rabson-Mendenhall syndrome - Insulin resistance Hypothalamic/ pituitary axes Pituitary Hyperpituitarism Acromegaly, Hyperprolactinaemia, SIADH Hypopituitarism Sheehan's syndrome, Kallmann syndrome, Growth hormone deficiency, Diabetes insipidus Adiposogenital dystrophy - Empty sella syndrome - Pituitary apoplexy - ACTH deficiency Thyroid Hypothyroidism Iodine deficiency, Cretinism, Congenital hypothyroidism, Goitre, Myxedema Hyperthyroidism Graves disease, Toxic multinodular goitre, Teratoma with thyroid tissue or Struma ovarii Thyroiditis De Quervain's thyroiditis, Hashimoto's thyroiditis, Riedel's thyroiditis Euthyroid sick syndrome - Thyroid hormone resistance - Thyroid nodule Parathyroid Hypoparathyroidism Pseudohypoparathyroidism - Hyperparathyroidism Primary, Secondary, Tertiary Adrenal Adrenocortical hyperfunction: Cushing's syndrome Nelson's syndrome, Pseudo-Cushing's syndrome - Hyperaldosteronism Conn syndrome, Bartter syndrome CAH Lipoid, 3β, 11β, 17α, 21α Adrenal insufficiency Addison's disease, Waterhouse-Friderichsen syndrome - Hypoaldosteronism Gonads ovarian Polycystic ovary syndrome, Premature ovarian failure testicular 5-alpha-reductase deficiency, 17-beta-hydroxysteroid dehydrogenase deficiency general Hypogonadism, Delayed puberty, Precocious puberty Other Androgen insensitivity syndrome - Autoimmune polyendocrine syndrome - Carcinoid syndrome - Gigantism - Short stature Laron syndrome, Psychogenic dwarfism - Multiple endocrine neoplasia 1, 2 - Progeria - Woodhouse-Sakati syndrome - thymus Abscess of thymus, Thymus hyperplasia see also congenital, neoplasia Retrieved from http://en..org/wiki/Hyperprolactinaemia Categories: NeuroendocrinologyHidden category: Articles needing additional references from December 2007 Views Article Discussion this page History Personal tools Log in / create account Navigation Main page Contents Featured content Current events Random article Search Go Search Interaction Community portal Recent changes Contact Donate to Help Toolbox What links here Related changes Upload file Special pages Printable version Permanent link Cite this page Languages Deutsch Español Norsk bokmål Polski This page was last modified on 25 June 2008, at 13:56
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