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58 Cards in this Set
- Front
- Back
Primary function of the neuroendocrine system
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to maintain body homeostasis through the manufacture and secretion of a variety of chemical mediators (hormones)
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A) what is it called when hormones exert their effects on distant sites?
B) when they diffuse through interstitial tissue and exert effects on adjacent sites? C) when they exert their effects on their own cell of origin? |
A) endocrine effects
B) paracrine effects C) autocrine effects |
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A) hydrophobic hormones
B) hydrophilic hormones |
A) steroids and thyroid hormones (cholesterol derivatives)-->diffuse through plasma membrane to help w/transcription of genes
B) all other hormones (amino acid derivatives) |
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Abnormalities of endocrine organs
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hyperfunction (abnormal stimulation, autonomous function, ectopic production)
hypofunction (congenital defect, acquired defect, end organ unresponsiveness) the local effects of an enlarging mass |
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Anterior pituitary hormones
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Growth hormone (GH)
Adrenal corticotropic hormone (ACTH) Follicle stimulating hormone (FSH) Lutenizing hormone (LH) Thyroid stimulating hormone (TSH) Prolactin (PL) |
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Posterior pituitary hormones
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Antidiuretic hormone (ADH, vasopressin)
Oxytocin These are found in the hypothalamus, then stored in the posterior pituitary |
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What is the most common basis of hyperpituitarism, and is usually due to a functional, benign, monoclonal neoplasm (pituitary adenoma) which secretes one of the polypeptide hormones?
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Autonomous pituitary hypersecretion
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What is the most common secretory product of pituitary adenomas?
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Prolactin excess
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Which hormone is responsible for exaggerated skeletal growth (giantism) before puberty and acromegaly (enlargement of face, hands, & feet) after puberty?
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Growth hormone excess
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What is the 2nd most common functional disorder of the pituitary?
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Acromegaly
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An increase in which hormone results in Cushing disease?
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ACTH
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Hypopituitarism most commonly results from what? What does this lead to?
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Extensive destruction of anterior lobe tissue
Leads to panhypopituitarism (Simmond disease) |
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Clinical features of Growth hormone (GH) deficiency (before and after puberty)
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before puberty-pituitary dwarfism (short stature with normal proportions) and delayed sexual maturity
after puberty-asymptomatic |
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Clinical features of Gonadotropin deficiency (in children, adult females, and adult males)
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children-delayed puberty
adult females-amenorrhea, loss of secondary sex characteristics, atrophy of ovaries and external genitalia adult males-aspermia, loss of secondary sex characteristics, testicular atrophy |
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Clinical features of TSH deficiency
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hypothyroidism
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Clinical features of ACTH deficiency
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Hypoadrenalism
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What is the most frequent cause of hypopituitarism?
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Non-functioning adenoma
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What does Sheehan Syndrome result from?
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Results from infarct of anterior lobe secondary to hypotension or shock.
Usually due to obstetric hemorrhage and hypotension |
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What is it called when, during pregnancy, the pituitary doubles in size, compromising the circulation, resulting in sudden hypotension and infarct? The first sign of this is failure to lactate or resume mences.
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Sheehan Syndrome
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An increase or decrease of which hormone does NOT have any associated clinical effects?
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Oxytocin
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A) What happens when you secrete excess ADH?
B) What happens when you don't make enough ADH? |
A) Syndrome of inappropriate ADH (SLADH)-renal retention of water and inability to dilute urine
B) Diabetes insipidus-symptoms similar to diabetes mellitus, and can be due to an end-organ unresponsiveness to the hormone |
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What is it called when expanding pituitary masses produce visual impairment by impinging the optic chiasm or compressing the oculomotornerves?
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Bitemporal hemianopsia
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What is the function of parafollicular or "C" cells?
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secrete the hormone calcitonin to oppose the effects of parathyroid hormone
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Thyroid hormones and functions
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T3 & T4 are released from the pituitary and have a negative feedback on the hypothalamus and pituitary
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Hyperthyroidism (thryotoxicosis)
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Hypermetabolic state produced by lots of T3 and/or T4. This is caused by Graves' disease, toxic multinodular goiter, and toxic adenoma,
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Hypothyroidism
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Deficiency of T3 and/or T4 and results from intrinsic thyroid disease (primary hypothyroidism) or TSH deficiency (secondary hypothyroidism)
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Late childhood or adult hypothyroidism (myxedema)
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Hypometabolic state characterized by tiredness, apathy, lethargy, slow speech, rough skin, and dilated heart.
Major causes: surgical, chemical, radiation, idiopathic myxedema, and Hashimoto thyroiditis |
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Gestational or early infancy hypothyroidism (cretinism)
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Arises from lack of iodine or defects in thyroid hormone synthesis. This may cause retardation, spasticity, and deaf-mutism (neurologic cretinism)
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Hashimoto thyroiditis
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Autoimmune disease in middle-aged women associated with hypothyroidism. The thyroid gland is enlarged, firm, and rubbery.
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Graves Disease (diffuse toxis gioter)
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Autoimmune disease in young, adult women associated with hyperthyroidism. Symptoms include enlarged thyroid, ocular changes(proptosis, diplopia, lid lag), and thickening of the skin over the feet and legs (pretibial myxedema)
The ocular changes are present in 70% of cases, but the skin changes are only present in 15%. |
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Goiter
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Enlargement of the thyroid gland
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Diffuse nontoxic goiter (simple/colloid goiter)
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Gradual, painless enlargement of the thyroid due to compensatory hyperplasia because of inability to secrete thyroid hormones.
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Multinodular gioter (adenomatous gioter)
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The end result of a long-standing diffuse nontoxic goiter, causing thryomegaly. They are more frequently seen in older females. Most of the time, the thyroid works fine (euthyroid). These are easily confused with cancer.
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What is the method for distinguishing a non-neoplastic nodule from a neoplastic nodule or a malignant nodule from a benign nodule?
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There is no method
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Benign neoplasms
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Adenomas arising from follicular epithelial cells. They become more frequent with age and are rarely functional. These have little malignant potential.
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Malignant neoplasms
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Relatively infrequent, but radiation exposure increases the risk. One nodule in a male is more likely malignant, but malignancy is higher in females.
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What is the most common thyroid malignancy?
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Papillary adenocarcinoma.
This is most present in young adult females. Surgery is needed to remove the entire thyroid, since it spreads by lymph nodes. This has a good prognosis. |
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Follicular carcinoma
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Most present in middle-aged females and grows slowly. The tumor spreads hematogenously to organs. There is a poor prognosis because it can differentiate.
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Parathyroid gland functions
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Regulate calcium metabolism
*This is opposed by the hormone calcitonin* |
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How is hyperparathyroidism relfected?
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By elevated PTH levels even in the face of hypercalcemia and increased urine calcium secretion.
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What is most frequent cause of primary hyperparathyroidism?
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A parathyroid adenoma, although parathyroid hyperplasia and ectopic production of PTH also occur.
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Hypoparathyroidism
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Characterized by low PTH and hypocalcemia. This is the result of parathyroidectomy.
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What is the function of mineralocorticoids (aldosterone)?
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Regulate extracellular fluid volume and potassium metabolism in the kidney
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Where are glucocorticoids (cortisol) produced and what is their function?
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Produced in the inner zone of the kidney and increase appetite, fat deposition in the face, protein breakdown, and impair inflammation and immunity.
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Excess mineralocorticoids
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Primary hyperaldosteronism (Conn Syndrome) is most often seen in middle-aged women and presents as moderate hypertension. This is caused by aldosterone-secreting cortical adenomas.
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Excess glucocorticoids (Cushing Syndrome)
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Relatively uncommon, but presents in middle-aged females.
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A) Primary hypercortisolism is associated with what?
B) Secondary hypercortisolism is associated with what? |
A) low serum ACTH
B) high serum ACTH |
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Excess androgens (adrenogenital syndromes)
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Uncommon, but may be inherited disorders that affect enzymatic activity in the steriodogenesis pathway, resulting in congenital adrenal hyperplasia.
Leads to precocious puberty in boys or masculinization of females |
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Primary chronic adrenocortical insufficiency (Addison disease)
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Results from a chronic destructive process that destroys 90% of the kidney's cortex.
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Secondary adrenocortical insufficiency
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Results from decreased ACTH secretion from the pituitary, causing lack of hyperpigmentation
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Acute adrenal insufficiency
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Life-threatening situation, resulting from sudden stress in patients with Addison disease or the abrupt withdrawal of exogenous steroidsa
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What makes up the Islets of Langerhans? What are their functions?
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Alpha cells (20%)-secrete glucagon (inhibits utilization of glucose)
Beta cells (70%)-secrete insulin (promotes utilization of glucose) Delta cells (5%)-secrete somatostatin (inhibits insulin and glucagon release) |
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What is the most common disease of the general population in the US, affecting 2% of people?
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Diabetes mellitus
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What is insulin and what is its function?
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An anabolic hormone involved in carb, protein, and lipid metabolism. It increases glucose rate of transport, promotes glycogen formation, converts glucose to triglycerides, and promotes nucleic acid and protein synthesis.
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Type I Diabetes (Juvenile onset, Insulin-dependent)
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15% of cases, results from inadequate insulin production and reduced number of beta cells in the pancreas.
Patients develop cytotoxic T cells and autoantibodies to beta cells, which are triggered by environmental factors. Health problems include ketoacidosis, retinal damage, kidney damage, vascular disease, and infection |
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Type II Diabetes (Adult onset, non-insulin dependent)
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Most common form of diabetes. Patients have deficient insulin secretion and end-organ resistance to insulin, are often obese, and have CV and kidney disease, nerve damage, and cataracts.
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Insulinoma (beta-cell tumors)
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Most common islet cell tumors. 10% are malignant.
Symptoms-hypoglycemia, stupor, loss of consciousness. These can be aborted by administering glucose. |
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Gastrinoma
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Tumors associated with gastric acid hypersecretion. Slightly over 50% are malignant.
Result in ulcers (Zollinger-Ellison syndrome) and fluid/electrolyte disturbance secondary to diarrhea and malabsorption. |