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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Once the individual stops growing then in general, so do the enchondromas. Case 7 Case 7.

Dyschondroplasia Ollier disease Prevalence: Se continuar a navegar, consideramos que aceita o seu uso. Case 2 Case 2. Ollier disease is not normally diagnosed until toddler years because it is not very visible. Loading Stack – 0 images remaining. Previous article Next article.

Nominally, the disease consists of multiple enchondromas which usually develop in childhood. The Spanish Association of Pediatrics has as one of its main objectives olljer dissemination of rigorous and updated scientific information on the different areas of pediatrics. Summary and related texts. Continuing navigation will be considered as acceptance of this use. If only a few bones are involved, then little if any handicap is present, although the affected bones do have a higher rate of fracture.

Print Send to a friend Export reference Mendeley Statistics. Are you a health professional enffrmedad to prescribe or dispense drugs? This section is empty. SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field. Persons with Ollier disease are prone to breaking bones and normally have swollen, aching limbs. Log in Sign up. Most patients have bilateral involvement but often significant asymmetry 4. You can also scroll through stacks with your mouse wheel or the keyboard arrow keys.


Achondrogenesis type 1B Autosomal recessive multiple epiphyseal dysplasia Atelosteogenesis, type II Diastrophic dysplasia.

Imagen de la semana. Infobox medical condition new Articles to be expanded from August All articles to be expanded Articles with empty sections from August All articles with empty sections Articles using small message boxes. Some authors make a distinction between Ollier disease and enchondromatosis on the basis olier distribution. X-ray image showing enchondromas localized in the lower part of the radius of a 7-year-old girl with Ollier disease.

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. With age, the cartilage may calcify in the typical “snowflake” pattern.

Ollier’s disease Ollier syndrome Multiple enchondromatosis Ollier’s syndrome Ollier disease. If involvement of the lower limbs is significant, leg length discrepancy may occur.

This page was last edited on 14 Octoberat Ollier disease is seen in both sexes without gender predilection and usually becomes apparent by early childhood 3,4.

enfermedad de Ollier – English Translation – Word Magic Spanish-English Dictionary

Metaphyseal dysplasia Jansen’s metaphyseal chondrodysplasia Schmid metaphyseal chondrodysplasia. Additional information Further information on this disease Classification s 4 Gene s 3 Clinical signs and symptoms Publications in PubMed Other website s 9. More interestingly, it has been reported that the PTHrP parathyroid hormone-related protein receptor has been implicated as a gene responsible for cases of enchondromatosis in patients with a family history of mild skeletal dysplasia in their male parents.

Lippincott Williams and Wilkins. SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact. Achondrogenesis type 2 Hypochondrogenesis. To improve our services and products, we use “cookies” own or third parties authorized to show advertising related to client preferences through the analyses of navigation customer behavior. A new clinical entity.


Ollier disease

Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. Case 8 Case 8.

Disease definition Enchondromatosis is a rare primary bone dysplasia disorder characterized by the development of multiple mainly unilateral or asymmetrically distributed enchondromas throughout the metaphyses of the long bones.

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 J Bone Joint Surg Am. Case 5 Case 5. Retrieved from ” https: You can help by adding to it. 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

Occasionally patients will also be afflicted with multiple osteochondromas. X-ray showing enchondromas localized in the lower part of the radius of a year-old patient affected with Ollier disease. In the entermedad description of Ollier disease, the enchondromas were predominantly confined to one side and limited to the limbs.

Juvenile granulosa cell tumour has been associated with the disease. Thank you for updating your details. Ollier disease is a rare nonhereditary sporadic disorder where intraosseous benign cartilaginous tumors enchondroma develop close to growth plate cartilage. 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.