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Maffucci syndrome life expectancy
People with Maffucci’s Syndrome usually live as long as others. This happens because the main characteristics of this condition are enchondromas (which are bone tumors) and hemangiomas (or skin bumps). These are often not cancerous and hardly ever impact crucial organs.
Ollier disease and maffucci syndrome
| Feature | Ollier Disease | Maffucci Syndrome |
|---|---|---|
| Growth of enchondromas | Typically one side of the body (arms, legs, hands, feet) | Both sides of the body |
| Hemangiomas | Absent | Present (reddish/purplish skin patches, sometimes internal) |
| Inheritance | Can be sporadic or inherited (rare) | Mostly sporadic |
| Appearance of symptoms | Usually childhood | Childhood or adolescence |
| Bone deformities | Common, often affecting hands and feet | Common, can affect various bones |
| Pain | Frequent | Frequent |
| Fractures | More likely due to weakened bones | More likely due to weakened bones |
| Risk of cancer | Small risk of enchondromas becoming cancerous | Slightly higher risk of enchondromas and hemangiomas becoming cancerous |
| Diagnosis | X-rays, CT scans | X-rays, CT scans, sometimes biopsy |
| Treatment | Pain management, surgery, monitoring | Pain management, surgery, monitoring, additional management for hemangiomas |
| Support | Support groups, online communities, medical professionals | Support groups, online communities, medical professionals |
Additional Notes:
- Both conditions are rare, affecting only a small number of people globally.
- Early diagnosis and management are crucial for both conditions.
- Living with Ollier disease and Maffucci syndrome can be challenging, but support and effective treatment can help individuals lead fulfilling lives.
Maffucci syndrome radiology
Doctors guess Maffucci’s Syndrome? They check with X-rays and CT scans. These scans like magic windows, reveal the two main culprits:
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