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Causes of hormonal alterations
- target cell fails to respond to hormone
- receptor-associated disorders
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Receptor associated disorders
- decreased # of receptors
- defective hormone-receptor binding
- impaired receptor functioning/insensitivity to hormone
- presence of antibodies against receptors that decrease available sites or mimic hormone action
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What type of disorder may involve inadequate synthesis of second messenger, such as cAMP, needed to signal intracellular events
intracellular disorders
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Target cell response for lipid soluble hormones (such as TH) occurs _______ often than water-soluble hormones (insulin)
less
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diseases of post. pituitary are usually r/t
abnormal ADH secretion
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SIADH is characterized by
high levels of ADH w/o normal physiologic stimulus for its release
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SIADH is associated with several forms of __________ because...
- cancer
- eptopic secreation of ADH by tumor cells
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main features of SIADH
- water retention and solute loss (especially Na+)
- leads to HYPOnatremia and HYPOosmalality
- Na+< 130
- thirst, impaired taste, anorexia, DOE, fatigue,dulled consiousness
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diabetes insipidus is r/t
insufficiency of ADH that leads to polyuria and polydipsia
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What happens in the neurogenic form of diabetes insipidus
organic leasion of hypothalamus or posterior pituitary interferes with ADH synthesis, transport, or release
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Diabetes insipidus risk factors
history of head injury, pituitary tumor, or craniotomy
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treatment for diabetes insipidus
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s&s of diabetes insipidus
- up to 20L urine/day
- low specific gravity
- low osmolarity
- hypovolemia
- increased thirst
- tachycardia
- low bp
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Nursing care for diabetes insipidus
- monitor fluids
- replace fluids
- check neuro stats and vitals
- check mucus membranes
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what causes the nephrogenic form of diabetes insipidus
insensitivity of renal tubules to ADH, particullarly the collecting tubules
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excessive urine output and low urine osmolality after a dehydration or water restriction test may require
ADH replacement with synthetic vasopressin
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Hypofunction of pituitary results from
- infarction of the gland
- removal or dstruction
- space-occupying pituitary adenomas or aneurysms compressing secreting pituitary cells
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what gland is extremely vascular and vulnerable to infarction
pituitary
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hyperfunction of pituitary caused by
adenoma composed of secretory pituitary cells
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panhypopituitarism
all hormones absent.
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panhypopituitarism results in
- cortisol deficiency (no ACTH)
- thyroid deficiency (no TSH)
- diabetes insipidus (no ADH)
- gonadal failure, loss of secondary sex characteristics, loss of libido (no FSH, LH)
- social withdrawl, fatigue, loss of motivation, osteoporosis (GH deficiency in adults)
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pituitary adenomas causing hyperpituitarism are usually
benign and slow growing tumors
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acromegaly in adults R/T
excess GH
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giantism in children whose epiphyseal plates have not closed r/t
excess GH
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prolactinomas related to
excessive gh
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most common form of hyperthyroid
graves disease
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hyperthyroid is likely associated with
autoimmune abnormalities
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opthalmopathy occurs in what percent of hyperthyroid cases
50-70%
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diffuse toxic goiter enlarges in response to
increased demand for TH
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thyroid storm can cause death within _______ w/o treatment
48 h
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Subacute thyroiditis
- nonbacterial inflammation preceded by viral infection
- hypo
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autoimmune thyroiditis is also known as
hashimoto disease
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hashimoto disease
thyroid destoryed by circulating thyroid antibodies and infiltration of lymphocytes
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subclinical hypothyroidism
elevated TSH with normal TH
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myxedema
- sign of sever or longstanding adult hypothyroid
- connective fibers separated by increaseing amount of protein and mucopolysaccharides wich binds water causing nonpitting edema (esp around eyes)
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thyroid carcinoma
most common endocrine malignancy but relatively rare
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hypothyroidism in infants b/c of absent thyroid tissue and hereditary defects in TH synthesis is what
cretinism
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if cretinism goes untreated
MR and stunted growth
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hypothyroidsm is difficult to id at birth but some symptoms are
- high birth weight
- low T
- delayed BM
- neonatal jaundice
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failed feedback mechanisms that cause increased PTH which causes hypercalcemia and decreased phosphate
primary hyperparathyroidism
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compensatory response to chronic hypocalcemia
secondary hyperparathyroidism
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loss of Ca+ with renal failure leads to increased secretion of
PTH
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causes excessive osteoclastic and osteolytic activity that results in bone resorption
hyperparathyroidism
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what is associated with insulin resistance, kidney stones, gi disturbances, muscle weakness, lethargy, dehydration
hyperparathyroid
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hypoparathyroidism is most commonly caused by
damage during thyroid surgery
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hypocalcemia causes
- tetany
- muscle spasms
- hyperreflexia
- clonic-tonic convultions
- laryngeal spasms
- death
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Type 1 DM
- lack of insulin
- excess glucose
- most common dx in whites
- peaks at 12 years
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heterogenous for HLA-DR3 and DR4 increases risk of type 1 dm
20-40 times
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which diabetes is ketosis prone
type 1
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decreased use of glucose accumulates in blood and releases in urine during
type 1 dm
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greatest risk factor of diabetes
obesity
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mass and number of beta cells decreased in
diabetes type 2
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hypoglycemic insulin shock level
below 60
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cushing syndrome
excessive levels of circulating levels of cortisol
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cushings disease
pituitary-dependent hypercortisolism due to an ACTH-secreating pituitary tumor
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without treatment, approx ______ of people with cushings die within 5 years b/c of
- 50%
- infection, suicide, HTN, atherosclerotic complications
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Conn disease is
primary aldosteronism
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most common cause of Conn diseae
benign, single adenoma followed by multiple tumors or hyperplasia
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symptoms of Conn disease
- HTN hypokalemia
- renal K+ wasting, neuromuscular manifestations
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hypocortisolsim
inadequate stimulation of adrenals by ACTH or inablitiy of adrenals to produce and secrete cortisol
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elevated serum ACTH levels with inadequate output
Addison disease
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phenochromocytoma causes
- hypersecretion of adrenal medulla
- excess production of epinephrine and norepi
- autoimmune function of tumor
- symptoms of persistant fight or flight
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