cushing s syndrome

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    CUSHINGS SYNDROME

    Roldan, Scorch Dominique

    Romero, John Reden

    Sanchez, Tracy Joy

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    DEFINITION

    Hormonal disorder caused by

    prolonged exposure of the bodys

    tissues to high levels of the

    hormone cortisol.

    Refers to excess cortisol of anyetiology

    Also known as hypercortisolism

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    FREQUENCY

    Relatively rare

    Most commonly affects

    adults aged 20 to 50.

    Women are three times

    more likely to develop thesyndrome than men.

    PREDISPOSING

    FACTOR

    Obesity

    Type II diabetes

    Individuals with poorly

    controlled blood sugar

    High blood pressure,

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    CHARACTERISTIC FEATURES

    Moon FaceTruncal obesity and thinextremities

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    CHARACTERISTIC FEATURES

    Buffalo humpPink or purple stretchmarks (striae)

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    OTHER SIGNS

    Thinning of scalp hair

    Acne

    Increased facial hair in women

    (hirsutism)

    Thinning, fragile skin that

    bruises easily

    Slow healing of cuts, insect bites

    and infections

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    PATHOPHYSIOLOGY

    Can be classified as:Endogenous Cushings syndrome

    Iatrogenic/Exogenous Cushings syndrome

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    Hypothalamus Anterior Pituitary Gland

    Cortisol Adrenal Glands

    CRH

    ACTH

    Cortisol

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    CortisolHypothalamus Anterior Pituitary Gland

    Cortisol Adrenal Glands

    CRH

    ACTH

    A pituitary gland tumor

    (pituitary adenoma)

    A noncancerous (benign) tumor of the

    pituitary gland, located at the base of

    the brain

    secretes an excess amount of ACTH,

    which in turn stimulates the adrenal

    glands to make more cortisol.

    When this form of the syndrome

    develops, it's called Cushing disease.

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    An ectopic ACTH-secreting tumor.

    The tumor develops in an organ that normally

    does not produce ACTH.

    The tumor will begin to secrete cortisol inexcess.

    These tumors, which can be noncancerous

    (benign) or cancerous (malignant), are usually

    found in the lungs, pancreas, thyroid or thymus

    gland.

    CortisolHypothalamus Anterior Pituitary Gland

    Cortisol Adrenal Glands

    CRH

    ACTH

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    Can be classified as: Iatrogenic/Exogenous Cushings syndrome

    Related to the use of corticosteroid medication

    PATHOPHYSIOLOGY

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    Corticosteroids contain a synthetic (man-made) version of the cortisol hormone.

    reduce inflammation in the body and suppresses the immune system

    Oral - The risk of developing

    Cushings syndrome is higher

    Autoimmune disease (Rheumatoid

    arthritis & Lupus)

    To prevent your body from

    rejecting a transplanted organ

    Topical

    Atopic eczema

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    Corticosteroids contain a synthetic (man-made) version of the cortisol hormone.

    reduce inflammation in the body and suppresses the immune system

    Injectable

    Joint pain

    Bursitis

    Back pain

    Inhaled

    Asthma

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    Because the doses required to treat

    these conditions are often higher than

    the amount of cortisol your bodynormally needs each day, the effects of

    excess cortisol can occur.

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    SYMPTOMSWomen with Cushing syndromemay experi

    Irregular or absent menstrual periods

    Men with Cushing syndromemay experience

    Decreased libido

    Decreased fertility

    Erectile dysfunction

    Other signs and symptomsinclude:

    Fatigue

    Muscle weakness

    Depression, anxiety and irritability

    Loss of emotional control

    Cognitive difficulties

    New or worsened high blood pressure

    Glucose intolerance

    Bone loss (osteoporosis)

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    COMPLICATIONS

    Bone loss (osteoporosis) unusual

    bone fractures, such as rib fractures and fracturesof the bones in the feet

    Glucose Intolerance Diabetes

    Pituitary Adenoma Panhypopituitarism

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    DIAGNOSIS 24-hour urinary free cortisol level.

    Midnight plasma cortisol measurements

    Late-night salivary cortisol measurements.

    Low-dose dexamethasone suppression test (LDDST).

    Imaging Test

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    24-hour urinary free cortisol level.

    a persons urine is collected several times over

    a 24-hour period and tested for cortisol.

    Levels higher than 50 to 100 micrograms a day

    for an adult suggest Cushings syndrome.

    Midnight plasma cortisol measurement

    measures cortisol concentrations in the blood.

    Cortisol production is normally suppressed at night,

    but in Cushings syndrome, this suppression doesnt

    occur.

    If the cortisol level is more than 50 nanomoles per

    liter (nmol/L), Cushings syndrome is suspected.

    DIAGNOSIS

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    Late-night cortisol measurement

    Low-dose dexamethasonesuppression test (LDDST). In the LDDST, a person is given a low dose of

    dexamethasone, a synthetic glucocorticoid, by mouthevery 6 hours for 2 days.

    Urine is collected before dexamethasone is administeredand several times on each day of the test.

    Cortisol and other glucocorticoids signal the pituitary torelease less ACTH, so the normal response after takingdexamethasone is a drop in blood and urine cortisollevels.

    If cortisol levels do not drop, Cushings syndrome issuspected.

    DIAGNOSIS

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    Imaging Test

    Computerized tomography

    scans or magnetic

    resonance imaging scans

    can provide images of your

    pituitary and adrenal

    glands to detectabnormalities, such as

    tumors.

    DIAGNOSIS

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    TREATMENT Reducing corticosteroid use

    Cortisol-Inhibiting Medications

    Surgery

    Radiotherapy

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    Reducing Corticosteroid use

    Cortisol- Inhibiting Medications

    are used on a long-term basis in

    people unwilling or unable to havesurgery.

    Most Widely used (Ketoconazole

    and Metyrapone)

    TREATMENT

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    Surgery Removal of tumor

    Removal of one of the adrenal glands

    Radiotherapy

    may be recommended if pituitary gland

    surgery is unsuccessful or if you

    are unable to have surgery. It involves

    using high-energy X-rays to shrink the

    tumour.

    TREATMENT