ENCONDROMATOSIS OLLIER PDF

Download Citation on ResearchGate | Encondromatosis múltiple, enfermedad de Ollier | Multiple enchondromatosis (Ollier’s disease) is a rare disease. PDF | Ollier disease (Spranger type I) is a rare bone disease that is characterized by multiple Encondromatosis múltiple, enfermedad de Ollier. Article. Enchondromatosis, also known as Ollier disease (see Terminology section), is a non-hereditary, sporadic, skeletal disorder characterised by multiple.

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Si continua navegando, consideramos que acepta su uso. C ] – Ovarian juvenile granulosa cell tumor with precocious pseudopuberty. Subscribe to our Newsletter. Ollier disease is not normally diagnosed until toddler years because it is not very visible.

Most cases of Ollier disease have been sporadic Halal and Azouz, However, 2 tumors with wildtype sequences from a subject with Maffucci syndrome oollier high levels of 2HG, and the third tumor with wildtype sequences, from a subject with multiple tumors subject 2had low levels of 2HG. By using this site, you agree to the Terms of Use and Privacy Policy.

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MRI showing enchondromas localized in the lower part of the radius of a year-old patient affected with Ollier disease.

Clinical problems caused by enchondromas include skeletal deformity and the potential for malignant change to osteosarcoma Schwartz et al.

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Enchondromatosis | Radiology Reference Article |

On radiographs, streaks of low density encondormatosis seen projecting through the diaphyses into the epiphyses of the long bones, due to ectopic cartilage deposits. Case 9 Case 9. X-ray of right leg AP and lateral views- multiple lytic expansile lesions in the metaphysis of femur, tibia and fibula. Enchondromas normally show a uniform pattern of mineralization.

Multiple Enchondromatosis: Olliers Disease- A Case Report

One tumor in subject 21 harbored a mutation causing an RS substitution, whereas the second tumor had wildtype sequences. Spondyloepiphyseal dysplasia congenita Multiple epiphyseal dysplasia Otospondylomegaepiphyseal dysplasia.

For further discussion of appearances, please refer to the article on enchondromas. We are determined to keep this website freely accessible.

Occasionally patients will also be olliwr with multiple osteochondromas. Related Radiopaedia articles Bone tumours 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. The magazine, referring to the Spanish-speaking pediatric, indexed in major international databases: Find articles by Sandeep Sadashiva.

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Ollier disease

Looking For More References? Support Radiopaedia and see fewer ads. Enchondromas econdromatosis common intraosseous tumours which are usually benign and develop in close proximity to growth plate cartilage.

Fourteen of 16 subjects had identical mutations in separate lesions.

Ollier disease – Wikipedia

X-ray image showing enchondromas localized in the lower part of the radius of a 7-year-old girl with Ollier disease. Case 3 Case 3. However, a differential of hereditary encondromxtosis needs to be ruled out. Case 5 Case 5. You can also scroll through stacks with your mouse wheel or the keyboard arrow keys. Discussion Olliers disease is characterized by the presence of at least three enchondromas [ 1 ].

Classification of the Enchondromatoses In their classification of the enchondromatoses, Spranger et al. Javier Tejada Gallego a. Fibromuscular dysplasia of intracranial arteries in a patient with enchondromas Ollier disease.

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