Dyschondroplasia Dyschondroplasia (enchondromatosis)(ollier s disease) Images.http//www.sbu.ac.uk/. Useful Link http//www.bdid.com/ollier.htm. http://www.e-radiography.net/radpath/d/dyschondroplasia.htm
Extractions: An enchondroma is a bit of cartilage (gristle) that has been left behind during the early development of a bone. As the bone lengthens, it gets dragged toward the shaft of a bone, where it begins growing on its own. They are probably not true tumors. The commonest site for enchondromas is the hands, followed by the feet and forearms. The skull, spine, and breastbone are seldom affected
Fox Mill Foot And Ankle Center > Ollier`s Disease You are in Foot Problems diseases of the Foot ollier`s disease. ollier`sdisease is usually associated with a bony prominence under the toenail. http://www.footdoctorva.com/prob_diseases_ollier.php
Ollier S Disease Complete online version of The Encyclopaedia of Medical Imaging including textand images from The Encyclopaedia of Medical Imaging s eight book volumes http://www.amershamhealth.com/medcyclopaedia/medical/Volume III 1/OLLIERS DISEAS
Ollier S Disease Complete online version of The Encyclopaedia of Medical Imaging including textand images from The Encyclopaedia of Medical Imaging s eight book volumes http://www.amershamhealth.com/medcyclopaedia/medical/Volume VII/OLLIERS DISEASE.
Case Of The Month - January, 2003 Multiple Enchodromatosis (ollier s disease) Discussion originally was describedby ollier in late 1800 s; - characterized by multiple enchondroma http://cases.pedrad.org/case.php?month=January&year=2003
Ollier's Disease - General Practice Notebook ollier s disease. This is a familial cause of multiple, unilateral chondromata.Click here for more information The information provided herein should http://www.gpnotebook.co.uk/cache/-1449525246.htm
Ollier's Disease - General Practice Notebook ollier s disease Patient UK www.patient.co.uk/showd ollier s disease PatientUK www.patient.co.uk/showd Image DermIS main menu DOIA Mafucci Syndrome http://www.gpnotebook.co.uk/medwebpage.cfm?ID=-1449525246
Journal Of Pediatric Orthopaedics B - UserLogin Maffucci lymphangioma syndrome an unusual variant of ollier s disease, Radiographs revealed ollier s disease (multiple enchondromas) involving the http://www.jpo-b.com/pt/re/jpedorthob/fulltext.01202412-200303000-00013.htm
Extractions: A case of Maffucci's syndrome in an 18-month old boy is presented, in which the vascular malformation consists of lymphangioma. This is a rare variant of Maffucci's syndrome. So far only six other cases have been reported in which lymphangiomas featured. We believe that the case described here is only the second case to be reported for which a lymphangioma is the only vascular malformation in the syndrome. The literature of the other six cases was reviewed and various features identified enabling this particular disease to be classified as a distinct variant of Maffucci's syndrome.
Clinical Nuclear Medicine - UserLogin ollier s disease Characteristic Tc99m MDP Scan Features ollier s diseaseis a rare, nonhereditary skeletal condition characterized by persisting http://www.nuclearmed.com/pt/re/cnm/fulltext.00003072-200301000-00017.htm
Blackwell Synergy - Cookie Absent She had been diagnosed as having enchondromatosis (ollier s disease) as a child . Enchondromatosis (ollier s disease) is a nonhereditary disorder of http://www.blackwell-synergy.com/doi/abs/10.1111/j.1471-0528.2004.00443.x
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Uhrad.com Pediatric Imaging Teaching Files Discussion Enchondromatosis (ollier s disease) is a non hereditary disorder ofenchondral ossification with lesions distributed throughout the tubular and http://www.uhrad.com/pedsarc/peds055.htm
Extractions: Click on Images for Enlarged View Clinical History: Trauma to second right digit. Findings: Multiple lucent metaphyseal lesions of the proximal and middle phalanges of the fourth and fifth digits, as well as the distal metacarpals of the fourth and fifth digits. Diagnosis: Multiple enchondromatosis. Discussion: Enchondromatosis (Ollier's Disease) is a non hereditary disorder of enchondral ossification with lesions distributed throughout the tubular and flat bones of the body. The presenting clinical manifestations are masses that increase in size as the child grows, asymmetric limb shortening and either genu varus or genu valgus deformities. Radiographs of the young child could be normal in the first few years of life and later demonstrate radiolucent streaking within the metaphysis of involved bones, or at infancy may demonstrate radiolucent masses which can be round, triangular or linear. Stippled calcifications occur with age within the enchondromas. There may be considerable expansion of the tubular bones especially in the hands, and pathologic fractures may occur. Cartilaginous areas extending from the physis can lead to a growth interference resulting in limb shortening and deformities. Enchondromas typically stabilize or regress in adulthood. However, sarcomatous transformation has been described. Six types of enchondromatosis have been described, of which three are more common. If the multiple enchondromas are purely unilateral or unevenly distributed throughout the metaphyses of the long bones, sparing the cranium and spine, it is called Ollier's Disease. If the enchondromas are seen with multiple cutaneous hemangiomas (soft tissue calcifications/phleboliths) it is called Maffucci's Syndrome. If there is symmetric involvement throughout the body including the cranium, hands and feet, it is known as generalized enchondromatosis. The Ollier's and Maffucci's are more common in boys (2:1). The less frequent types include metachondromatosis which affects the short tubular bones of the hands and feet, and spondyloenchondroplasia in which the enchondromas are associated with platyspondyly, and enchondromas with irregular vertebral bodies.
Extractions: SARCOMATOUS TRANSFORMATION OF the enchondromas is a well-known complication of Ollier's disease, and nonsarcomatous malignancies have usually been associated with Maffucci's syndrome. Only 13 cases of multiple enchondromatosis associated with intracranial gliomas have been described, 5 of which were in patients with Ollier's disease. We describe three patients, including identical twins, who had both Ollier's disease and primary brain tumors. This is the first report of Ollier's disease in identical twins. These three cases support the theory that Ollier's disease and Maffucci's syndrome may represent a spectrum of the same disease process rather than two distinct diseases.
Discussion Message Display ollier s disease was posted 06/26/1998 0937 am by Becksmom1@AOL.com some webresearch and it appears to me to actually be more like ollier s disease. http://162.129.103.56/N/n.web?EP=N&URL=/MCGI/SEND1^WEBUTLTY(200,25980)/125100803
