ENFERMEDAD DE OLLIER PDF

These manuscripts contain updated topics with a major clinical or conceptual relevance in modern medicine. The journal adheres to the standards of academic research publications in all aspects including peer-review and ethical principles. 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. CiteScore measures average citations received per document published. Read more.

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These manuscripts contain updated topics with a major clinical or conceptual relevance in modern medicine. The journal adheres to the standards of academic research publications in all aspects including peer-review and ethical principles.

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. CiteScore measures average citations received per document published.

Read more. SRJ is a prestige metric based on the idea that not all citations are the same. SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal's impact.

SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field. ISSN: Previous article Next article. Issue 3. Pages e5 June Imagen de la semana. Ollier's disease. Maria Rexach Fumanya. Corresponding author. This item has received. Article information. Subscriber If you already have your login data, please click here. More information. From Monday to Friday from 9 a. Subscribe to our newsletter. Print Send to a friend Export reference Mendeley Statistics.

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Ollier disease

Alternative titles; symbols. They can occur as solitary lesions or as multiple lesions in enchondromatosis. When hemangiomata are associated, the condition is known as Maffucci syndrome Clinical problems caused by enchondromas include skeletal deformity and the potential for malignant change to osteosarcoma Schwartz et al. In their classification of the enchondromatoses, Spranger et al. Halal and Azouz added 3 tentative categories to the 6 in the classification of Spranger et al.

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Some authors make a distinction between Ollier disease and enchondromatosis on the basis of distribution. In the original description of Ollier disease, the enchondromas were predominantly confined to one side and limited to the limbs. 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. Ollier disease is seen in both sexes without gender predilection and usually becomes apparent by early childhood 3,4,. The condition is non-hereditary and is thought to occur as a result of random and spontaneous mutations. Clinical presentation is usually with deformity and pain present only during periods of rapid growth 3,4.

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Ollier disease is a rare sporadic nonhereditary skeletal disorder in which typically benign cartilaginous tumors enchondromas develop near the growth plate cartilage. This is caused by cartilage rests that grow and reside within the metaphysis or diaphysis and eventually mineralize over time to form multiple enchondromas. These symptoms are typically first visible during early childhood with the mean age of diagnosis being 13 years of age. Currently, there are no forms of treatment for the underlying condition of Ollier disease but complications such as fractures, deformities, malignancies that arise from it can be treated through surgical procedures. The prevalence of this condition is estimated at around 1 in ,

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