Maffucci’s Syndrome: Characteristics, and Radiology
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
FeatureOllier DiseaseMaffucci SyndromeGrowth of enchondromasTypically one side of the body (arms, legs, hands, feet)Both sides of the bodyHemangiomasAbsentPresent (reddish/purplish skin patches, sometimes internal)InheritanceCan be sporadic or inherited (rare)Mostly sporadicAppearance of symptomsUsually childhoodChildhood or adolescenceBone deformitiesCommon, often affecting hands and feetCommon, can affect various bonesPainFrequentFrequentFracturesMore likely due to weakened bonesMore likely due to weakened bonesRisk of cancerSmall risk of enchondromas becoming cancerousSlightly higher risk of enchondromas and hemangiomas becoming cancerousDiagnosisX-rays, CT scansX-rays, CT scans, sometimes biopsyTreatmentPain management, surgery, monitoringPain management, surgery, monitoring, additional management for hemangiomasSupportSupport groups, online communities, medical professionalsSupport 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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