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50 Cards in this Set
- Front
- Back
MCC of Cushing's syndrome
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exogenous (iatrogen) steroid use (decreased ACTH)
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Cushing's disease
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70% of endogenous causes; due to ACTH secretion from pituitary adenoma (increased ACTH)
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ectopic ACTH as cause of Cushing's
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15%; nonpituitary tissue making ACTH ex. small cell lung cancer, bronchial carcinoids (increased ACTH)
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adrenal cause of Cushing's
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15%; adenoma, carcinoma, nodular adrenal hyperplasia (decreased ACTH)
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dexamethasone suppression test - healthy person
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decreased cortisol level after low dose
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dexamethosone suppression test - ACTH producing pituitary tumor (Cushing's disease)
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increased cortisol after low dose; decreased cortisol after high dose
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dexamethosone suppression test - ectopic ACTH producing tumor
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increased cortisol after both low and high doses
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dexamethasone suppression test - cortisol-producing tumor
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increased cortisol after low and high dose
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clinical findings in Cushing's syndrome
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HTN, weight gain, moon facies, truncal obesity, buffalo hump, hyperglycemia, skin changes, osteoporosis, amenorrhea, immune suppression
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primary hyperaldosteronism (Conn's syndrome)
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unilateral/bilateral aldosterone-secreting tumor
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findings in Conn's syndrome
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hypertension (Na+ and H20 retention), hypokalemia, metabolic alkalosis (H+, K+ secretion), low plasma renin
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treatment of Conn's syndrome
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(1) surgery to remove tumor (2) spirinolactone - K+ sparing diuretic that is an aldosterone antagonist
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secondary hyperaldosteronism
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kidney perception of low IV volume results in overactive renin-angiotensin system; associated with high plasma renin
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causes of secondary hyperaldosteronism
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CHF, renal artery stenosis, chronic renal failure, cirrhosis, nephrotic syndrome
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Addison's disease
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chronic primary adrenal insufficiency due to adrenal atrophy or destruction by disease resulting in deficiency of aldosterone and cortisol
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findings in Addison's disease
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hypotension, hyperkalemia, metabolic acidosis, skin hyperpigmentation, adrenal atrophy of all 3 layers
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secondary adrenal insufficiency
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decreased pituitary ACTH production which has no skin hyperpigmentation and no hyperkalemia
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waterhouse-friedrichson syndrome
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acute primary adrenal insufficiency due to adrenal hemorrhage
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causes of waterhouse friedrichson syndrome
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Neisseria meningitidis, DIC, endotoxic shock
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MC tumor of adrenal medulla in adults
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pheochromocytoma
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which cells does a pheochromocytoma arise from?
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chromaffin cells (neural crest)
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findings in pheochromocytoma
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(1) episodic HTN - due to E, NE and DA release (2) urinary VMA elevated (3) plasma catecholamines elevated
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pheochromocytomas are associated with..
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neurofibromatosis, MEN types 2a and 2b
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rule of 10s (pheochromocytoma)
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10% malignant, 10% bilateral, 10% extraadrenal, 10% calcify, 10% kids, 10% familial
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pheochromocytoma symptoms
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episodic: Pressure (BP), Pain (headache), Perspiration, Palpitations (tachycardia), Pallor
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breakdown productions of DA (1), NE (2) and E (3)
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(1) DA - HVA (2) NE - VMA (3) E - metanephrine
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MC tumor of adrenal medulla in children
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neuroblastoma
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neuroblastoma
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can occur anywhere along sympathetic chain, elevated HVA in urine, overexpression of N-myc oncogene associated with rapid tumor progression
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signs/symptoms of hypothyroidism
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cold intolerance, weight gain (decreased appetite), lethargy/fatigue, constipation, decreased reflexes, myxedema, dry cool skin, bradycardia, dyspnea on exertion
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signs/symptoms of hyperthermia
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heat intolerance, weight loss, increased appetite, hyperactivity, diarrhea, increased reflexes, pretibial myxedema, warm moist skin, fine hair, chest pain, palpitations, arrhythmias
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lab findings in hypothyroidism
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increased TSH, decreased total T4, free T4, T3 uptake
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lab findings in hyperthyroidism
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decreased TSH, increased total T4, freeT4 and T3 uptake
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MCC of hypothyroidism
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Hashimoto's thyroiditis
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Hashimoto's thyroiditis
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autoimmune disorder; antimicrosomal and antithyroglobulin ab's with association to HLA-DR5
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histology in Hashimoto's
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Hurthle cells, lymphocytic infiltrate with germinal centres
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findings in Hashimoto's
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moderately enlarged, nontender thyroid
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Cretinism
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severe fetal hypothyroidism
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endemic Cretinism
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endemic goiter is prevalent ex. lack of dietary iodine
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sporadic cretinism
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defect in T4 formation or developmental failure in thyroid function
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findings in Cretinism
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pot bellied, pale, puffy-faced child with protruding umbilicus and protuberant tongue; mental retardation
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subacute thyroiditis (de Quervain's)
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self-limited hypothyroidism following a flu-like illness; may initially be hyperthyroid
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histology of subacute thyroiditis
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granulomatous inflammation
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findings in subacute thyroiditis
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increased ESR, jaw pain, early inflammation, very tender thyroid
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Reidel's thyroiditis
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thyroid replaced by fibrous tissue (hypothyroid)
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findings in Riedel's thyroiditis
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fixed, hard (rock-like) and painless goiter
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Grave's disease
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type II HS, autoimmune hyperthyroidism with thyroid stimulating/TSH receptor antibodies
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signs/symptoms of Grave's disease
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ophthalmopathy - proptosis, EOM swelling; pretibial myxedema, diffuse goiter; often presents during stress
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thyrotoxicosis
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stress-induced catecholamine surge leading to death by arrhythmia; serious complication of Grave's disease
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toxic multinodular goiter
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focal patches of hyperfunctioning follicular cells working independently of TSH due to mutation of TSH receptor; increased release of T3/T4
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Jod-Basedow phenomenon
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thyrotoxicosis if a patient with iodine deficiency goiter is made iodine replete
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