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38 Cards in this Set
- Front
- Back
MCC of nonmalignant hypercalcemia?
MCC by? |
Primary hyperparathyroidism (HPTH)
- mcc by parathyroid adenoma (80% of cases) |
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HPTH associated with what?
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MEN 1 and MEN2a
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What is net GI absorption of Ca/day
Ca is 45% protein bound... which protein is it mostly bond to? |
200mg
- mostly bound to albumin |
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Primary regulator of serum calcium
What amount of serum Ca causes max secretion of this primary regulator? |
PTH
- Ca drops below 7.5 mg/dl causes max release of PTH |
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for every serum albumin decrease of 1g/dl what is change in serum Ca?
How does a tourniquet effect serum Ca? |
decrease of .8mg/dl
- tourniquet causes transductino of plasma water (but not protein) into tissue which elevates total serum Ca |
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In parathyroid adenoma what is MC gland effected?
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usually right inferior
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Role of pH and Ca change
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Ph. The binding of Ca to protein increases with ph. A change of 0.1 ph unit causes an opposite change of 0.12 mg/dl in the ionized Ca.
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What drugs cause hypercalcemia/
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vit D, A, lithium, thiazide diuretics, calcium- containing antacids (milk-alkali syndrome)
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One of the causes of primary hyperparathyroidism is primary hyperplasia...
Which glands are affected and which cells? What are other cells associated and what is name? |
usually all four glands
usually seen in chief cell hyperplasia - sometimes clear cell hyperplasia (aka wasserhelle cell hyperplasia)--> With this you will see markedly increased serum calcium levels |
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What group of people tend to more frequently have primary hyperparathyroidism?
MC presentation? |
post menopausal women (show hypercalcemia)
- MC presentation is asymptomatic |
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What are granulomatous causes of hypercalcemia?
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Sarcoidosis, tuberculosis and histoplasmosis elevate 1,25- vitamin D3 levels via activated monocytes
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Acute kidney failure can cause hypercalcemia how?
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Hypercalcemia may occur in the polyuric recovery phase of acute
tubular necrosis due to elevated PTH and 1,25-vit.D3 levels and dissolution of ectopic ( usually muscle ) calcium phosphate deposits. |
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MC see in dialysis patients or women undergoing treatment for osteoporosis as cause of hypercalcemia?
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Vit D intoxication
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Milk-alkali syndrome caused by (in relation to hypercalcemia)
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caused by ingestion of large amount of Ca ( > 5g/day ) and alkali. Alkalosis increases protein binding of Ca and stimulates tubular calcium reabsorption
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3 main ways hypercalcemia may occur with malginancies?
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1. MC 2ndary to osteolytic lesions (metastatic breast, and multiple meyloma) phosphate elevated
2. Other neoplasms (lymphomas) synthesize excessive amount of 1,25 dihydroxyvitamin D... elevated phosphate 3. Ectopic production of PTH-related peptide) (Squamous, renal, bladder, ovarian cancers) secrete PTH like hormone so PTH should be depressed |
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How does sarcoidosis cause hypercalcemia?
Clinically shown as? |
macrophages in granulomas synthesize 1a-hydroxylase causing hyper vit. D
- seen hilar adenopathy, rash, lymphadenopathy, EKG abnormalities |
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Acute hypercalcemia steps of treatments?
What are anti-responsive steps? |
1. correct dehydration, induce calciuria with saline diuresis (w or w/o loop diureti 2 to 6L/d)
2. Institute antiresponsive therapy if doesnt work a. First line0 pamidronate disodium 90 mg IV (bisphosphanate) b. Adjunctive: synthetic salmon calcitonin 100-400 U c. secondline- etidronate disodium, gallium nitrate |
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When is surgery indicated for primary hyperparathyroidism?
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1. Serum Ca >11.5mg/dl
2. Nephrolithiasis 3. Compromized renal function (CrCl <70%) 4. Hyper calcinuria (>400 mg Ca/day) 5. osteoporosis (T-score < -2.5) 6. age <50 yo |
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What clinical signs do you show with hypercalcemia caused by malignancy
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often weight loss, anorexia and Serum Ca levels above 15 mg/Dl (3.75 mmol/L)
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What is cause of Familial benign hypocalciuric hypercalcemia?
When would you suspect it? and how do you dx? |
mutation in parathyroid calcium receptors FBHH must be
- suspected in patients whose urinary Ca/ creatinine clearance ratio is less than 0.01 ( fasting morning spot urine collection), confirmed by finding hypercalcemia in a first- degree relative, 50% of whom carry the trait - excluded in patients with mild asymptomatic hypercalcemia because it requires no treatment and does not respond to subtotal parathyroidectomy |
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Clinical findings of hypocalcemia
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tingling in lips and finger tips
tetany, muscle cramps, tetany, psychosis, abnormal cardiac function (CHF, hypotension, prolongation of QT interval, ventricular conduction defects, resists Dig) |
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MCC of hypocalcemia in chemotherapy pt?
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secondary to acute calcium complexation due to hyperphosphatemia caused by tumor lysis syndrome
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Most common cause of hypoparathyroidism and other main causes
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1. autoimmune
2. surgical previously removed thyroid 3. DiGeourge Syndrome- 4. Hypomagnesemia |
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How does low magnesium cause hypoparathyroidism?
Causes of hypomagnesemia? |
Mg is cofactor for adenylate cyclase which activates cAMP and cAMP is required for PTH
- caused by diarrhea, aminoglycosides, diuretics, alcoholism |
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If pt produces PTH but has hypocalcemia... and no renal failure what might they have most likely?
How does this type of pt present? What are their Phosphate? D3? Vit. D? |
AD disease of pseudohypoparathyroidism- where organs are resistant to PTH
- mental retardation, short forth and fifth metacarpals - decreased phosphate and vit. D but normal D3 |
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What is the knuckle, knuckle, dimple dimple sign? Pathopneumonic for?
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means short fourth and fifth digits seen in pesudohypoparathyroidism
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How does acute pancreatitis cause hypocalcemia?
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Ca is bound to FA in enzymatic fat necrosis... very poor sign
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Why does low Ca cause tetany?
What is clinical signs? |
decreased ionized Ca level which lowers threshold potential (Et) to near resting membrane potential (Em)
- it takes much less effort to activate - thumbs adduct into palm, facial twitching after tapping facial nerve |
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If pt has following features with no signs of calcium disorder its known as?
– Short stature – Round face – Short neck – Short metacarpals and metatarsals (brachydactyly) – Mental retardation |
The skeletal abnormalities in the absence of any calcium disorder - “
pseudopseudohypoparathyroidism” |
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Following features with Ca disorder known as
– Short stature – Round face – Short neck – Short metacarpals and metatarsals (brachydactyly) – Mental retardation |
pseudohypoparathyroidism
- "Albrights hereditary osteodystrophy" results from kidney unresponsiveness to PTH |
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First step in Differential diagnosis of hypocalcemia
Why measure albumin, pH, and Mg? |
verify true hypocalcemia measure ionized Ca
- measure serum albumin and pH to exclude pseudo hypocalcemia and acute respiratory alkalosis - Mg- low Mg decreases PTH secretion and leads to resistance to PTH action on bone |
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Hypocalcemia with high phosphorus
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rhabdomyolysis,
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low phosphorus, high PTH, low Ca most likely?
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Vit D def, pancreatitis or metastatic bone disease
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low Ca, high PTH, high phosphorus think?
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rhabdomyolysis, chronic renal insufficiency and pseudohypoparathyroidism (this results from end organ resistance to PTH)
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low Ca and low or normal PTH thinking?
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If low or normal - hypoparathyroidism is present. PTH deficiency can result from absence of functional tissue owing to surgical removal, replacement by tumor or infiltration with amyloid.
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What conditions cause decreased D3 production?
loss of D3? |
liver disease,
- accelerated loss of 25- OH D3 because of the nephrotic syndrome or abnormalities of the enterohepatic circulation. |
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alkaline phosphatase levels in the following...
a. vit D def b. renal failure |
both high
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tx of hypocalcemia?
What if acute symptomatic? |
1. Treat underlying cause
2. Ca supplementation 3. Vit supplementation 4. If acute symptomatic requires immediate tx preferred by 10-20 ml Ca gluconate (90mg Ca per 10 ml vial) at no more than 2ml/min. or CaCl (272 mg Ca per 10 ml vial) |