Bone Disease Flashcards

(32 cards)

1
Q

What is the definition of Osteoporosis?

A

Metabolic bone disease characterised by low bone mass and micro architectural deterioration of bone leading to increased risk of fractures, the bone is 2.5 SD away from being healthy

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2
Q

What are the secondary causes of osteoporosis?

A
Hyperparathyroidism 
Gh deficiency 
Malabsorption 
Malignanc 
Rheumatic drugs 
Amenorrhea
Oestrogen Deficiency
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3
Q

What is the pathogenesis of osteoporosis?

A

Increased breakdown by osteoclasts and decreased production by osteoblasts

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4
Q

What is the presentation of Osteoporosis?

A

Fractures on low impact
Asymptomatic
Crushed vertebra Colles’s fractures

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5
Q

What is the GOLD standard investigation on osteoporosis? What does this scan look at?

A

Dexa Bone Scan

Bone mineral density

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6
Q

What are some other investigations to do in osteoporosis?

A

Plain radiograph

FBC’s

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7
Q

What are the prophylactic measures in OP?

A

HRT
Physiotherapy
Stop smoking and alcohol
Calcium and vitamin D for those on steroids

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8
Q

What are the 4 medical management options for osteoporosis?

A
Biphosphonates
Vitamin D/ calcium 
Raloxifene
Strotium ranelate
Risk factor assessment
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9
Q

What is Rickets?

A

Severe vitamin D or calcium nutritional deficiency in children
Before the epiphyseal plates have closed

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10
Q

What is osteomalacia?

A

Severe vitamin D or calcium nutritional deficiency in Adults
After the epiphyseal plates have closed

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11
Q

What is the most common cause of rickets?

A

Lack of phosphate or vitamin D deficiency

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12
Q

What are the clinical features of rickets?

A

Stunted growth, curve in the spine, wide bones

Bowed legs

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13
Q

What are the clinical features of Osteomalacia?

A

Joint and bone pain, muscle weakness, abnormal gait, low calcium features = irregular heart, numbness and muscle spasms

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14
Q

what are your investigations for these 2?

A

Serum Vit D, Calcium, phosphate, PTH
X-ray
Bone biopsy

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15
Q

What are the managements?

A

Oral calcium and vitamin D

Bone correction surgery

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16
Q

What is Pagets Disease?

A

This is a disorder of bone remodelling after an initial event of excessive reabsorption, this leads to disorganised bone with more vascualtoyt and less compact meaning it can be fractures more easily

17
Q

What are the causes of Paget’s disease?

A

This is familial in 30%

Can be caused by an environmental trigger

18
Q

What bones are most commonly involved?

A

Femoral, pelvis and skull

19
Q

What is the presentation of Paget’s disease

A
This is a condition in the over 40's, who have:
Bone pain and deformity 
Excessive heat over the bone 
Neurological complications 
Can be complicated by osteosarcoma
FH of pagers disease
20
Q

What is THE diagnostic test in pagets disease?

A

Raised SERUM ALKALINE PHOSPHATASE
Bone Scan
X-ray/ bon biopsy

21
Q

What is the management of Paget’s bone disease?

A

Minimal unless skull involvement

IV biphosphonate

22
Q

What is osteogenesis Imperfecta

A

This is genetic connective tissue disorder where there is very fragile bones form mild trauma and daily living

23
Q

What are the 4 types of OI?

A

1 = mild, presents in adults
Type 2 = can be lethal by age 1
3 = more severe and progressive
4 = adults but very severe very quickly

24
Q

What re the clinical features of OI?

A
Growth deficiency 
Defective tooth formation 
Hearing loss
Blue sclera
Barrel chest
Easy bruising 
OI
25
What is the clinical diagnosis and management of OI?
Skin biopsy and genetic testing | IV biphosphonates and that the fractures surgically
26
What is Marfan's syndrome?
This is an autosomal DOMINANT condition in which there is loss of the elastic tissue
27
What is the cause of Marfan's syndrome?
This is due to a defect in the fibrillar gene
28
What are the 3 diagnostic areas that are affected in Marfan's syndrome?
MSK Cardio Occular
29
What MSK symptoms are seen in Marfan's syndrome?
``` Caved chest Long and Thin limbs Scoliosis Thumb sign Back ache ```
30
What ocular symptoms are seen in Marfan's syndrome?
Myopia and retinal detachment
31
What Cardio symptoms are seen in Marfan's syndrome?
Aortic aneurysm - Dilatation/ dissection Aortic/mitral valve murmur Pneumothorax
32
What are the managements for Marfan's Syndrome?
``` Antihypertensives Aortic root Sx Mechanical valve insertion Surgery for ocular symtoms Myopia = corrective lens Physio and analgesia ```