Disorders of Calcium Metabolism Flashcards

1
Q

Calcium distribution

A
  • Bones & teeth (~99%)
  • ICF (~1%)
  • ECF (<1%)
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2
Q

Calcium Sensor Receptor activation effects

A

Parathyroid Cell -PTH Secretion Parafollicular C-Cell -Calcitonin Secretion Renal Tubular Cell -Calcium Excretion

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3
Q

Primary Hyperparathyroidism Classification

A
  • Adenoma85%
  • Hyperplasia15%
  • Carcinoma< 1%
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4
Q

Primary Hyperparathyroidism Clinical Features

A

-Asymptomatic (> 50%)
-Skeletal Disease
-Kidney Disease
-Gastrointestinal Disease
-Psychiatric Disease
-Band Keratopathy
(Bones Stones Groans Moans)

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5
Q

Signs of Hyperparathyroidism

A
  • Brown Tumor (Osteoclastoma)
  • Osteitis Fibrosa Cystica
  • Chondrocalcinosis
  • Band Keratopathy
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6
Q

Lab findings in Primary Hyperparathyroidism

A

Inc Serum Calcium
Dec Serum Phosphate
Inc Serum PTH

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7
Q

Genetic causes of Primary Hyperparathyroidism

A
Sporadic90% 
Familial10% 
-Familial HPT 
-MEN I 
-MEN IIA
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8
Q

MEN 1 features & mutation

A
  • Pituitary tumors
  • Pancreatic Islet Tumors
  • Parathyroid Hyperplasia
  • Germline Mutation: Menin Gene
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9
Q

MEN 2a features & mutation

A
  • Medullary Thyroid Carcinoma
  • Pheochromocytoma
  • Parathyroid Hyperplasia
  • Germline mutation: RetGene (GDNF receptor)
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10
Q

Primary Hyperparathyroidism Treatment

A
  • Surgery
  • CalcimimeticDrug (Cinacalcet)
  • Anti-ResorptiveBone Drug (Bisphosphonate, Denosumab)
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11
Q

Most common causes of hypercalcemia

A
  1. Primary Hyperparathyroidism

2. Hypercalcemia of malignancy

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12
Q

WHEN DO you find increased PTH

A

FHH & primary hyperparathyridism

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13
Q

Hypercalcemia of Malignancy Mediators

A

PTH Related Peptide (PTH-RP)

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14
Q

Lab findings in Hypercalcemia of Malignancy

A

Inc Serum Calcium
Low Serum PTH
Inc Serum PTH-RP

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15
Q

Familial Hypocalciuric Hypercalcemia lab findings

A

Inc Serum Calcium (mild)
High Serum PTH (mild)
Low Urinary Calcium (defective receptor/excretion in kidney)
Low Urine Calcium / Creatinine Clearance Ratio

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16
Q

Hypocalcemia Causes

A
Vitamin D Deficiency
Hypoparathyroidism (only one w/ low PTH)
Pseudohypoparathyroidism
Hypomagnesemia 
Hypoproteinemia**
17
Q

Corrected Serum Total Calcium method

A

Add 0.8 mg/dl to total Calcium for every 1 g/L Albumin is < 4.0 g/L

18
Q

Hypocalcemia Clinical Features

A
Paresthesias
Muscle Cramps
Muscle Weakness
Chvostek’s Sign
Trousseau’s Sign
19
Q

Major Storage Form of Vitamin D

A

25 OH Vitamin D

20
Q

Vitamin D Disorders

A
  • Acquired Vitamin D Deficiency (Intake probs, no sun)
  • Acquired 1,25 (OH)2 Vitamin D Deficiency (Renal Disease Hypoparathyroidism)
  • Congenital 1 Alpha Hydroxylase Deficiency “Vitamin D Dependent Rickets Type 1”
  • Congenital Vitamin D Receptor Deficiency “Vitamin D Dependent Rickets Type 2”
21
Q

Nutritional Vitamin D Deficiency Lab findings

A
Low Serum Calcium
 low Serum Phosphate 
highSerum Alkaline Phosphatase 
high Serum PTH 
low Serum 25 (OH) Vitamin D
low urine Calcium
22
Q

Clinical features of Vit D deficicny

A

Osteomalacia –Pseudofracture

23
Q

Hypoparathyroidism Laboratory Features

A

Low Serum Calcium
High Serum Phosphate
Low Serum PTH

24
Q

Pseudohypoparathyroidism Causes

A

Inactivating mutation of the GS alpha subunit or other downstream PTH response element

25
Q

Pseudohypoparathyroidism Laboratory Features

A
  • low Serum Calcium
  • high Serum Phosphate
  • high Serum PTH
  • Short 4th + 5th Metacarpals (Albright’s Hereditary Osteodystrophy)