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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Javier Tejada Gallego a. 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.

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. By using this site, you agree to the Terms of Use and Privacy Policy. You can change the settings or obtain more information by clicking here. Support Radiopaedia and see fewer ads.


Most patients have bilateral involvement but often significant asymmetry 4.

Show all Show less. X-ray image showing enchondromas localized in the lower part of the radius of a 7-year-old girl with Ollier disease. Lippincott Williams and Wilkins. Persons with Ollier ollirr are prone to breaking bones and normally have swollen, aching limbs. You can change the settings or obtain more information by clicking here.

For all other comments, please send nefermedad remarks via contact us. In the original description of Ollier disease, the enchondromas were predominantly confined to one side and limited to the limbs.

Orphanet: Enfermedad de Ollier

Articles Cases Courses Quiz. Ollier disease is seen in both sexes without gender predilection and usually becomes apparent by early childhood 3,4. J Bone Joint Surg Am. CiteScore measures average citations received per olllier published.

SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field. Achondroplasia Hypochondroplasia Thanatophoric dysplasia.



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Ollier disease

Case 7 Case 7. X-ray showing calcified ebfermedad localized in finger a year-old patient affected with Ollier disease. 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 The growth of these enchondromas usually stops after skeletal maturation.

Loading Stack – 0 images remaining. Other search option s Alphabetical list. Si continua navegando, consideramos que acepta su uso. If involvement of the lower limbs is significant, leg length discrepancy may occur. Ollier disease is not normally diagnosed until toddler years because it is not very visible.