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Cushing syndrome

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Cushing syndrome
Hypercortisolism A condition characterized by excess corticosteroids, due either to an hypersecretion of cortisol by a hyperfunctioning or neoplastic adrenal cortex, or due to exogenous corticosteroids Etiology Exogenous coticosteroid administration; less commonly, pituitary hyperplasia, adenomas, or cancer Clinical Amenorrhea, hirsutism, HTN, impotence, muscular wasting, skin atrophy, neuropsychiatric dysfunction, osteoporosis, truncal–central obesity, weight gain–water retention, moon face, weakness, fatigue, backache, headache, ↑ thirst, ↑ urination, DM, osteoporosis Lab Hypersecretion of cortisol, loss of the usual circadian rhythm of ACTH and cortisol, and loss of suppressibility of cortisol production by administration of dexamethasone; ↑ adrenal androgens suppresses pituitary output of LH and FSH and causes ↓ sperm production or ovulatory failure Management Surgical excision if tumor is ID'd. See Dexamethasone suppression test, Ectopic hormone syndrome. Cf Pseudo-Cushing syndrome.


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While adrenal carcinoma accounts for only approximately 5-10% of cases of Cushing syndrome; approximately 40% of patients with both Cushing syndrome and an adrenal mass have a malignant tumour (2, 3).
Children experience cognitive decline despite reversal of brain atrophy one year after resolution of Cushing syndrome.
Chronic liver disease like in Hemochromatosis, endocrine abnormalities like in Hyperthyroid and Cushing syndrome are very common.
 
 
 
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