ENFERMEDAD DE OLLIER PDF

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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X-ray showing calcified enchondromas localized in finger a year-old patient affected with Ollier disease.

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Enchondromatosis | Radiology Reference Article |

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. 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. Ollier disease X-ray image showing enchondromas localized in the lower part of the radius of a 7-year-old girl with Ollier disease.

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. X-ray image showing enchondromas localized in the lower part of the radius of a 7-year-old girl with Ollier disease.

The extent of disease is highly variable and thus so is the degree of impairment. Prevalence is estimated at around 1 inX-ray showing enchondromas localized in the humerus of a year-old patient affected with Ollier disease. The magazine, referring to the Spanish-speaking pediatric, indexed in major international entermedad Si continua navegando, consideramos que acepta su uso.

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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. Most patients have bilateral involvement but often significant asymmetry 4. Juvenile granulosa cell tumour has been associated with the disease. Radiographs show multiple enchondromas. In the original description of Ollier disease, the enchondromas were predominantly confined to one side and limited to the limbs.

In distinction from solitary lesions, enchondromas of enchondromatosis are more likely to be hypercellular ehfermedad nature, yet are still considered benign in the absence of other aggressive findings If growth occurs then, this raises the possibility of malignant transformation 4.

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Ollier disease is not normally diagnosed until toddler years because it is not very visible. June Pages e5-e6 Pages snfermedad From Monday to Friday from 9 a. These manuscripts contain updated topics with a major clinical or conceptual relevance in modern medicine. Subscribe to our Newsletter.

Some authors make a distinction between Ollier disease and enchondromatosis on the basis of distribution. Case 1 Case 1. The growth of these enchondromas usually stops after skeletal maturation. Print Send to a friend Export reference Mendeley Statistics.

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Ollier disease – Wikipedia

Specialised Social Services Eurordis directory. Case 6 Case 6. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used enfermedas a basis for diagnosis or treatment.

Achondrogenesis type 1B Autosomal recessive multiple epiphyseal dysplasia Atelosteogenesis, type II Diastrophic dysplasia. If involvement of the lower limbs is significant, leg length discrepancy may occur.

Ollier disease

CiteScore measures average citations received per document published. 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.

Synonyms or Alternate Spellings: Summary and related texts. The etiology of enchondromatosis has been associated with post-zygote state mutations during development. On radiographs, streaks of low density are seen projecting through the diaphyses ollisr the epiphyses of the long bones, due to ectopic cartilage deposits.

By using this site, you agree to the Terms of Use and Privacy Policy. They can occur anywhere but most frequently involve the short tubular enfermwdad of the hands and feet.