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38 Cards in this Set

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MCC of nonmalignant hypercalcemia?

MCC by?
Primary hyperparathyroidism (HPTH)
- mcc by parathyroid adenoma (80% of cases)
HPTH associated with what?
MEN 1 and MEN2a
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
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
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
In parathyroid adenoma what is MC gland effected?
usually right inferior
Role of pH and Ca change
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.
What drugs cause hypercalcemia/
vit D, A, lithium, thiazide diuretics, calcium- containing antacids (milk-alkali syndrome)
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
What group of people tend to more frequently have primary hyperparathyroidism?
MC presentation?
post menopausal women (show hypercalcemia)

- MC presentation is asymptomatic
What are granulomatous causes of hypercalcemia?
Sarcoidosis, tuberculosis and histoplasmosis elevate 1,25- vitamin D3 levels via activated monocytes
Acute kidney failure can cause hypercalcemia how?
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.
MC see in dialysis patients or women undergoing treatment for osteoporosis as cause of hypercalcemia?
Vit D intoxication
Milk-alkali syndrome caused by (in relation to hypercalcemia)
caused by ingestion of large amount of Ca ( > 5g/day ) and alkali. Alkalosis increases protein binding of Ca and stimulates tubular calcium reabsorption
3 main ways hypercalcemia may occur with malginancies?
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
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
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
When is surgery indicated for primary hyperparathyroidism?
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
What clinical signs do you show with hypercalcemia caused by malignancy
often weight loss, anorexia and Serum Ca levels above 15 mg/Dl (3.75 mmol/L)
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
Clinical findings of hypocalcemia
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)
MCC of hypocalcemia in chemotherapy pt?
secondary to acute calcium complexation due to hyperphosphatemia caused by tumor lysis syndrome
Most common cause of hypoparathyroidism and other main causes
1. autoimmune
2. surgical previously removed thyroid
3. DiGeourge Syndrome-
4. Hypomagnesemia
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
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
What is the knuckle, knuckle, dimple dimple sign? Pathopneumonic for?
means short fourth and fifth digits seen in pesudohypoparathyroidism
How does acute pancreatitis cause hypocalcemia?
Ca is bound to FA in enzymatic fat necrosis... very poor sign
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
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”
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
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
Hypocalcemia with high phosphorus
rhabdomyolysis,
low phosphorus, high PTH, low Ca most likely?
Vit D def, pancreatitis or metastatic bone disease
low Ca, high PTH, high phosphorus think?
rhabdomyolysis, chronic renal insufficiency and pseudohypoparathyroidism (this results from end organ resistance to PTH)
low Ca and low or normal PTH thinking?
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.
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.
alkaline phosphatase levels in the following...
a. vit D def
b. renal failure
both high
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)