Difference between revisions of "Joint Response to Injury"
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| + | ===Causes of injury === | ||
| + | |||
| + | *Trauma | ||
| + | *Instability | ||
| + | *Lubrication failure | ||
| + | *Infectious organisms | ||
| + | *Immune-mediated disease | ||
| + | |||
| + | ===Reaction to injury=== | ||
| + | |||
| + | *[[Joints - normal#Articular cartilage|Articular cartilage]] has limited ability to regenerate | ||
| + | **Superficial defects are long standing | ||
| + | ***Chondrocyte hyperplasia is ineffective at filling the defect | ||
| + | ***Non-painful | ||
| + | **Defects reaching subchondral bone | ||
| + | ***Filled with vascular fibroous tissue undergoing [[General Pathology - Disorders of Cell Growth#Metaplasia|metaplasia]] into cartilage | ||
| + | ***Painful | ||
| + | **Fibrillation - loss of proteoglycans -> condensation of collagen fibres -> fraying of surface | ||
| + | **Eburnation - loss of articular cartilage -> exposure of subchondral bone -> becomes dense and polished | ||
| + | *Synovial membranes respond by: | ||
| + | **Villous hypertrophy | ||
| + | ***+/- [[Joints - inflammatory|synovitis]] | ||
| + | **Hyperplasia | ||
Revision as of 19:43, 18 August 2008
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Causes of injury
- Trauma
- Instability
- Lubrication failure
- Infectious organisms
- Immune-mediated disease
Reaction to injury
- Articular cartilage has limited ability to regenerate
- Superficial defects are long standing
- Chondrocyte hyperplasia is ineffective at filling the defect
- Non-painful
- Defects reaching subchondral bone
- Filled with vascular fibroous tissue undergoing metaplasia into cartilage
- Painful
- Fibrillation - loss of proteoglycans -> condensation of collagen fibres -> fraying of surface
- Eburnation - loss of articular cartilage -> exposure of subchondral bone -> becomes dense and polished
- Superficial defects are long standing
- Synovial membranes respond by:
- Villous hypertrophy
- +/- synovitis
- Hyperplasia
- Villous hypertrophy