Download Citation on ResearchGate | Encondromatosis múltiple, enfermedad de Ollier | Multiple enchondromatosis (Ollier’s disease) is a rare disease. Request PDF on ResearchGate | Enfermedad de Ollier: tumores benignos con riesgo de malignización. Revisión de 17 casos | AimTo review. Ollier disease is a skeletal disorder characterized by multiple enchondromas, which are noncancerous (benign) growths of cartilage that develop within the.
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Most patients have bilateral involvement but often significant asymmetry 4.
Ovarian cancer 2nd ed. Achondrogenesis type 2 Hypochondrogenesis. The growth of these enchondromas usually stops after skeletal maturation. From Wikipedia, the free encyclopedia. Case 4 Case 4. This item has received. Juvenile granulosa cell tumour has been associated with the disease. SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact. Case 7 Case 7. If pain occurs when the child is older, this should raise the concern of malignant transformation or pathological fracture.
Views Read Edit View history. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment. Case 5 Case 5. Subscribe to our Newsletter. Print Send to a friend Export reference Mendeley Statistics. In distinction from solitary lesions, enchondromas of enchondromatosis are more likely to be hypercellular in nature, yet are still considered benign in the absence of other aggressive findings Nominally, the disease consists of multiple enchondromas which usually develop in childhood.
Health care resources for this disease Expert centres Diagnostic tests 14 Patient organisations 50 Orphan drug s 0.
Enfermedad de Ollier | Medicina Clínica
Case 3 Case 3. Articles Cases Courses Quiz. Ollier’s disease Ollier syndrome Multiple enchondromatosis Ollier’s syndrome Ollier disease. Detailed information Article for general public Svenska About Blog Go ad-free.
Prevalence is estimated at around 1 inThe documents contained in this web site are presented for information purposes only.
Imagen de la semana. Maffucci syndrome carries a higher risk for cancer. Radiographs show multiple enchondromas. Lippincott Williams and Wilkins. D ICD – Osteochondroma osteochondromatosis Hereditary multiple exostoses.
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Clinical presentation is usually with deformity and pain present only during periods of rapid growth 3,4. MRI showing enchondromas localized enfermedaf the lower part of the radius of a year-old patient affected with Ollier disease.
The condition is non-hereditary and is thought to occur as a result of random and spontaneous mutations. Loading Stack – 0 images remaining. Ollier disease is a rare nonhereditary sporadic disorder where intraosseous benign cartilaginous tumors enchondroma develop close to growth plate cartilage. Spondyloepiphyseal dysplasia congenita Multiple epiphyseal dysplasia Otospondylomegaepiphyseal dysplasia.
Persons with Ollier disease are prone to breaking bones and normally have swollen, aching limbs. For all other comments, please send your remarks via contact us.
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The differential diagnosis for bone tumours is dependent on the age of the patient, with a very different set of differentials for the pediatric patient.
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