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Description Cushing's syndrome is the result of the excessive production of corticosteroids by the adrenal glands. An overproduction of corticotrophin (the hormone that controls the adrenal gland) by the pituitary gland , which stimulates the adrenal glands to produce corticosteroids, may be one cause. In addition, certain lung cancers and other tumours outside the pituitary gland may produce corticotrophins. Other causes include benign or cancerous tumours on the adrenal glands. Symptoms and Signs The most common symptoms may include:
However, each individual may experience symptoms differently. Diagnosis and Treatment In addition to a complete medical history and medical examination, diagnostic
procedures for Cushing's syndrome may include x-rays to locate any tumours;
24-hour urinary test to measure for corticosteroid hormones; CAT scan
to detect any abnormalities that may not show up on an ordinary x-ray;
MRI; dexamethasone suppression test - to differentiate
whether the excess production of corticotrophins are from the pituitary
gland or tumours elsewhere; corticotropin-releasing
hormone (CRH) stimulation test - to differentiate whether the cause
is a pituitary tumour or an adrenal tumour. Description Tumours of the adrenal glands are rare. However, when present, they can cause a multitude of disorders by excessively secreting certain adrenal-produced hormones. One type of tumour of the adrenal glands is called a pheochromocytoma . A pheochromocytoma is a benign adrenal gland tumour that secretes adrenaline (epinephrine) and noradrenaline (norepinephrine) hormones. These hormones are responsible for regulating heart rate and blood pressure, among other functions. Pheochromocytomas occur most frequently in young to middle-aged adults between the ages of 30 and 60.
The information in this page is presented in summarised form and has been taken
from the following source(s):
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http://www.hon.ch/Dossier/MotherChild/child_hormones/cushings_syndrome.html | Last modified: Jun 25 2002 |