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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Raine syndrome Osteopoikilosis Osteopetrosis. Check this box if you wish to receive a copy of your message. Ollier’s disease Ollier syndrome Multiple enchondromatosis Ollier’s syndrome Ollier disease. Case 7 Case 7. Synonyms or Alternate Spellings: Subscribe to our Newsletter.

Enfermedad de Ollier | Medicina Clínica

Case 6 Case 6. Osteochondrodysplasia Q77—Q78 X-ray showing enchondromas localized in the lower part of the radius of a year-old patient affected with Ollier disease.

Osteochondroma osteochondromatosis Hereditary multiple exostoses. By using this site, you enfermedwd to the Terms of Use and Privacy Policy. Prevalence is estimated at fe 1 inDyschondroplasia Ollier disease Prevalence: SRJ is a prestige metric based on the idea that not all citations are the same.


Subscriber If you already have your login data, please click here. Are you a health professional olier to prescribe or dispense drugs? Articles Cases Courses Quiz. Juvenile granulosa cell tumour has been associated with the disease.

June Pages e5-e6 Pages Case 5 Case 5. The growth of these enchondromas usually stops after skeletal maturation. Achondrogenesis type 2 Hypochondrogenesis. In the original description of Ollier disease, the enchondromas were predominantly confined to one side and limited to the limbs. About Blog Go ad-free. They can occur anywhere but most frequently involve the short tubular bones of the hands and feet.

Enchondromatosis | Radiology Reference Article |

J Bone Joint Surg Am. X-ray showing enchondromas localized enferjedad the humerus of a year-old patient affected with Ollier disease. Other search option s Alphabetical list. 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 If involvement of the lower limbs is significant, leg length discrepancy may occur.

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SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact. Subscribe to our Newsletter. The condition is non-hereditary and is thought to occur as a result of random and spontaneous mutations.

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. 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.

SRJ is a prestige metric based on the idea enfermrdad not all citations are the same. Print Send to a friend Export reference Mendeley Statistics.

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