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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These manuscripts contain updated topics with a major clinical or conceptual relevance in modern medicine. Juvenile granulosa cell tumour has been associated with the disease. X-ray showing enchondromas enfermeedad in the lower part of the radius of a year-old patient affected with Ollier disease. Subscribe to our Newsletter. 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.
Ee deformities are managed surgically to preserve the function of the limb. SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact.
Print Send to a friend Export reference Mendeley Statistics. Related Radiopaedia articles Bone tumours 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. Some authors make a distinction between Ollier disease and enchondromatosis on the basis of distribution. SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field.
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Enchondromatosis | Radiology Reference Article |
Only comments seeking to improve the quality and accuracy of information on wnfermedad Orphanet website are accepted. Ollier’s disease Ollier syndrome Multiple enchondromatosis Ollier’s syndrome Ollier disease. Ovarian cancer 2nd ed. Metaphyseal dysplasia Jansen’s metaphyseal chondrodysplasia Schmid metaphyseal chondrodysplasia.
The Impact Factor measures the average number of citations received in a particular year by papers published in the journal during the two receding years. The documents contained in this web site are presented for information purposes only.
Ollier disease ejfermedad a rare nonhereditary sporadic disorder where intraosseous benign cartilaginous tumors enchondroma develop close to growth plate cartilage.
Case 5 Case 5. Raine syndrome Osteopoikilosis Osteopetrosis.
Detailed information Article for general public Svenska Continuing navigation will be considered as acceptance of this use. Maffucci syndrome carries a higher risk for cancer.
Case 3 Case 3.
Imagen de la semana. The Impact Factor measures the average number of citations received in a particular year by papers published in the journal during the two receding years.
Enfermedad de Ollier | Medicina Clínica
The magazine, referring to the Spanish-speaking pediatric, indexed in major international databases: Enchondromatosis is a rare primary bone dysplasia disorder characterized by the development of multiple mainly unilateral or asymmetrically distributed enchondromas enferedad the metaphyses of the long bones.
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If involvement of the lower limbs is significant, leg length discrepancy may occur. About Blog Go ad-free. Additional information Further information on this disease Classification s 4 Gene s 3 Clinical signs and symptoms Publications in PubMed Other website s 9.
You can also scroll through stacks dw your mouse wheel or the keyboard arrow keys. SRJ is a prestige metric based on the idea that not all citations are the same. Articles Cases Courses Quiz. From Monday to Friday from 9 a.
Nominally, the disease consists of multiple enchondromas which usually develop in childhood. As such, some authors prefer to use the term Ollier disease in cases where this distribution is present and use enchondromatosis or multiple enchondromatosis for cases where the distribution is more symmetric 5.
Case 2 Case 2. Are you a health professional able to prescribe or dispense drugs? MRI showing enchondromas localized in the lower part of the radius of a year-old patient affected with Ollier efnermedad. Achondroplasia Hypochondroplasia Thanatophoric dysplasia. CiteScore measures average citations received per document published. Log in Sign up. Case 4 Case 4.