Medical

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.

Author: Arashisida Mirn
Country: Cayman Islands
Language: English (Spanish)
Genre: Photos
Published (Last): 11 July 2013
Pages: 497
PDF File Size: 5.76 Mb
ePub File Size: 17.13 Mb
ISBN: 465-7-93215-588-1
Downloads: 53572
Price: Free* [*Free Regsitration Required]
Uploader: Kazrar

Synonyms or Alternate Spellings: Juvenile granulosa cell tumour has been associated with the disease.

In distinction from solitary lesions, enchondromas of enchondromatosis are more likely to be hypercellular in nature, pllier are still considered benign in the absence of other aggressive findings Continuing navigation will be considered as acceptance of this use. Annals of Pediatrics is the Body of Scientific Expression of the Association and is the vehicle through which members communicate.

The growth of these enchondromas usually stops after skeletal maturation.

Si continua navegando, consideramos que acepta su uso. Specialised Social Services Eurordis directory. Thank you for updating your details. Maffucci syndrome carries a higher risk for cancer.

Enchondromatosis | Radiology Reference Article |

Imagen de la semana. Multiple enchondromatosis, Ollier disease.

  ROQUE CORDERO CURSO DE SOLFEO PDF

CiteScore measures average citations enfermedqd per document published. The documents contained in enfer,edad web site are presented for information purposes only. Case 4 Case 4. 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. X-ray showing enchondromas localized in the lower part of the radius of a year-old patient affected with Ollier disease.

Only comments written in English can be processed.

Statistics

Raine syndrome Osteopoikilosis Osteopetrosis. Engermedad from ” https: Se continuar a navegar, consideramos que aceita o seu uso. MRI showing enchondromas localized in the lower part of the radius of a year-old patient affected with Ollier disease. The material is in no way intended to ollifr professional medical care by a qualified specialist and should not be used as a basis for diagnosis or enfermmedad.

You can help by adding to it. If pain occurs when the child is older, this should raise the concern of malignant transformation or pathological fracture. These manuscripts contain updated topics with a major clinical or conceptual relevance in modern medicine. Achondrogenesis type 1B Autosomal recessive multiple epiphyseal dysplasia Atelosteogenesis, type II Diastrophic dysplasia.

Professionals Summary information Greekpdf Review article English You can change the settings or obtain more information by clicking here. Case 1 Case 1.

  ABIES WEBBIANA PDF

If only a few bones are involved, then little if any handicap ebfermedad present, although the affected bones do have a higher rate of fracture. Support Radiopaedia and see fewer ads. Case 6 Case 6.

Persons with Ollier disease are prone to breaking bones and normally have swollen, aching limbs. 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. If involvement of the lower limbs is significant, leg length discrepancy may occur.

Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted. Once the individual stops growing then in general, so do the enchondromas.

SRJ is a prestige metric based on the idea that not all citations are the same. The condition is non-hereditary and is thought to occur as a result of random and spontaneous mutations.