Osteomalacia Flashcards

1
Q

What is osteomalacia

A

A disorder of mineralisation foo bone matrix (osteoid)

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2
Q

What is Rickets

A

a disorder of defective mineralisation of cartilage in the epiphyseal growth plates of children

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3
Q

Describe the aetiology of osteomalacia

A

Osteoclasts begin the bone remodelling cycle by excavating a cavity on the bone surface
Osteoblasts lay down the organic matrix (osteoid)

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4
Q

What are matrix vesicles

A

Extracellular organelles derived from the plasma membrane of chondrocytes

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5
Q

What is defective bone mineralisation in osteomalacia mostly due to

A

reduced calcium and phosphate elevel sin the extracellular fluid

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6
Q

When can primary renal phosphate wasting occur

A

Renal tubular acidosis
X linked hypophosphataemic rickets
autosomal dominant hypophosphataemic rickets
oncogenic (tumour-induced) osteomalacia

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7
Q

How might osteomalacia present radiologically

A

as osteopenia

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8
Q

What might patients with osteomalacia complain of

A

Diffuse bone pain and tenderness
fractures with little or no trauma
proximal muscle weakness - associated with a waddling gait

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9
Q

What are some other skeletal deformities in children with Ricket’s

A

Frontal bossing
pectus carinatum
bowing of the long bones

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10
Q

What investigations should be done for suspected osteomalacia

A

spine X ray - increased bone density

Looser’s zones or pseudo fractures (characteristic finding)

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11
Q

How can osteomalacia be diagnosed

A

bone biopsy using double tetracycline labelling

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12
Q

What is the treatment for osteomalaicia

A

Reversal of the underlying disorder (eg. gluten free diet)

Supplementation with vitamin D and calcium

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13
Q

How are patients with hereditary hypophosphataemic rickets treated

A

with a combination of oral phosphate supplementation and calcitriol

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14
Q
Describe the following in patients with vitamin D deficiency  
Plasma phosphate
plasma calcium 
alkaline phosphatase 
25-hydroxyvitamin D
PTH
A
Plasma phosphate: low
plasma calcium: low
alkaline phosphatase: increased
25-hydroxyvitamin D: low 
PTH: increased
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15
Q

How are patients with hereditary hypophosphataemic rickets treated

A

a combination of oral phosphate supplementation and calcitriol

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16
Q

What often indicates that treatment is effective in hypocalcaemic patients

A

Maintenance of normal urinary calcium levels