Xray2000 Dyschondroplasia (enchondromatosis)(ollier s disease). Definition A rarely familial, proliferation of cartilage in the metaphyses http://www.xray2000.f9.co.uk/radpath/d/dyschondroplasia.htm
Ollier's Disease (www.whonamedit.com) If you, or anybody close to you, is affected, or believe to be affected, by any condition mentioned here see a doctor. ollier s disease http://www.whonamedit.com/synd.cfm/1813.html
Extractions: This survey of medical eponyms and the persons behind them is meant as a general interest site only. No information found here must under any circumstances be used for medical purposes, diagnostically, therapeutically or otherwise. If you, or anybody close to you, is affected, or believe to be affected, by any condition mentioned here: see a doctor. A disorder of the growing ends of bones in which round nonossified cartilaginous masses scattered throughout the skeleton produce asymmetrical and very variable deformities, asymmetric leg shortening being common. The lesions are first noted from 1 to 4 years of age, rarely at birth, with little progression after adolescence. Both sexes may be affected. The majority of cases have been sporadic but a familial tendency has been reported in a few instances. Enchondromatosis is usually bilateral. The term Ollier syndrome applies in cases with unilateral involvement. The combination of multiple enchondromata with haemangiomata and phleboliths is known as Maffucci syndrome.
Louis Xavier Édouard Léopold Ollier (www.whonamedit.com) Associated with KlippelTrénaunay-Weber syndrome,ollier s disease,ollier s layer,ollier-Thiersch graft. Who named it? Home. List categories. olliers disease. http://www.whonamedit.com/doctor.cfm/477.html
Extractions: This survey of medical eponyms and the persons behind them is meant as a general interest site only. No information found here must under any circumstances be used for medical purposes, diagnostically, therapeutically or otherwise. If you, or anybody close to you, is affected, or believe to be affected, by any condition mentioned here: see a doctor. Louis Xavier Édouard Léopold Ollier is particularly remembered for his work on bone and joint surgery. He was born in Vans, Ardèche, where both his father and his grandfather had been doctors. He initially studied natural science at Montpellier and in 1849 was assistant in botany in the faculty of medicine.
Ollier's Disease ollier s disease. by Christina Gentle ArticleInsider.com % If brender = 0 Then % Check Out Our Suggested Site for ollier s disease Information! % End If % . http://www.deformitydepot.com/olliers-disease.html
Extractions: ArticleInsider.com Ollier's disease is a defect which can be present from birth, but is not hereditary, that causes tumors to grow in the bones usually on one side of the body. Generally the long bones are affected like the femur or tibia, for example, and can also affect bones in the feet and hands. Tumor growth in the bones, caused by this disease can affect the growth plates, and if this occurs in one of the legs it can lead to a leg length discrepancy. Check Out Our Suggested Site for Ollier's Disease Information! An example case can be a child who shows signs of this disease by walking with a limp, and when observed more closely it may be noticed that one leg is shorter than the other. This occurrence can be a result of unossification, caused by Ollier's, which is when bone stops forming normally. In this particular form limb lengthening procedures can be performed to help lengthen the shorter leg to a close proximity of the longer one. Factors of Ollier's Disease The lumping and swelling which can occur around infected areas of bone can lead to outward lesions and can become infected if not cared for properly. Tumors around the bones in children with this disease are most likely benign, but in adults with other conditions the tumors can lead to malignant transformations. Deformities other than leg length discrepancy can appear, and when bones become very weak in children, fractures can become common.
Ollier's Disease Other characters, ollier s disease,. Print this article, (Louis ollier, 18301900, French orthopaedic surgeon), enchondromatosis multiple. http://www.amershamhealth.com/medcyclopaedia/Volume VII/OLLIERS DISEASE.asp
Ollier's Disease N, O, P, Q, R, S, T, U, V, W, X, Y, Z, Other characters, ollier s disease,. Print this article, (Louis ollier, 18301900, French orthopaedic surgeon), enchondromatosis multiple. http://www.amershamhealth.com/medcyclopaedia/medical/Volume VII/OLLIERS DISEASE.
Birth Disorder Information Directory - O Lethal Type See Young McKeever Squier Syndrome. ollier s disease (Dyschondroplasia, Multiple Enchodromatosis, Osteochondromatosis) http://www.bdid.com/defecto.htm
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 http://www.gpnotebook.co.uk/cache/-1449525246.htm
Ollier's Disease - General Practice Notebook ollier s disease. Medical search. This is a familial cause of multiple, unilateral chondromata. http://www.gpnotebook.co.uk/medwebpage.cfm?ID=-1449525246
Extractions: Founded in 1998, incorporated in 2002 as a not-for-profit corporation and registered as a tax exempt organization with the US Internal Revenue Service, AAMED is comprised of individuals with Ollier's disease, Maffucci's syndrome, enchondromatosis, their families, and physicians. AAMED is THE source for news and information about bone tumor diseases, research and services for adults and children with Enchondromatosis, Multiple Enchondroma, Ollier's disease, Maffucci's syndrome, and their families. On this site, you'll find links to our quarterly newsletters, message board, pen-pal program for children, latest research information, and much more. We invite interested persons to become part of group. Click on the membership link for more information on joining us. participation in research projects to find treatments and a cure for these diseases helping families cope with the physical/psychological burdens imposed by the disease we provide a forum for patients and families to express their concerns and experiences connect individuals with common symptoms and backgrounds we continuously update a data base of physicians and hospitals with Ollier/Maffucci expertise Videos on limb lengthening and the use of the Ilizarov fixator
Ollier's Disease : On Medical Dictionary Online ollier s disease defined on the Free Online Medical Dictionary. ollier s disease. Benign growths of cartilage in the metaphyses of several bones. http://www.online-medical-dictionary.org/?q=Ollier's Disease
Wheeless' Textbook Of Orthopaedics Main Menu Home Page Multiple Enchodromatosis (ollier s disease). Discussion The malignant potential of enchondromatosis ollier s disease. An http://www.wheelessonline.com/o6/93.htm
Extractions: Main Menu Home Page - Discussion: - originally was described by Ollier in late 1800's; - characterized by multiple enchondroma lesions primarily located w/ in the metaphyseal regions of tubular bones; - usually diagnosed in childhood; - pts w/ Ollier's dz have increased risk of a secondary chondrosarcoma developing later in life; - risk is about 25% by age 40 yrs; - Clinical Findings: - most pts have bilateral involvement, w/ predominance on one side; - enchondromas most frequently involve the short tubular bones of hands - Radiographs: - in most cases, there will be diaphyseal lesions or metaphyseal lesions which do not cross the growth plate, at least, not until growth plate closure; - in some cases enchondromatosis will affect patients in the metaphyseal and epiphyseal regions; - when enchondromas cross the growth plate, severe limb length deformities and angular deformities will develop; The malignant potential of enchondromatosis Ollier's Disease. An assessment of angular deformity, shortening, and
Entrez PubMed Click here to read Malignant progression in multiple enchondromatosis (ollier s disease) an autopsybased molecular genetic study. http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=1
Uhrad.com Pediatric Imaging Teaching Files Discussion Enchondromatosis (ollier s disease) is a non hereditary disorder of enchondral 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.
Musculoskeletal Diseases Enchondromatosis. About ollier s disease xray2000.co.uk. ollier/Maffucci Self Help Group - (US). ollier s disease Self Help Group, UK. Fibrous Dysplasia of Bone. http://www.mic.ki.se/Diseases/C05.html
Extractions: Diseases and Disorders Links pertaining to Musculoskeletal Diseases Alert! Patients and laypersons looking for guidance among the target sources of this collection of links are strongly advised to review the information retrieved with their professional health care provider. Start Page Contents: Achondroplasia Achondroplasia Acquired Hyperostosis Syndrome Acrocephalosyndactylia ... Tietze's Syndrome Musculoskeletal Diseases Textbook of Orthopaedics [CR Wheeless] Educational textbook syllabus [Borrill et al.] - Orthoteers (UK) The Belgian OrthoWeb - (BE) Site Map of the Orthopaedics and Sports Medicine resource at Univ of Washington, Seattle (US) The American Academy of Orthopaedic Surgeons A Musculoskeletal Atlas and a set of educational cases (radiol.) - U of Washington (US) OrthoLinx WorldOrtho including A Simple Guide to Orthopaedics [RL Huckstep] - Nepean Hosp., Sydney (AU) A collection of Case discussions at OrthoGate.org An orthopedic Encyclopedia - for patients - DynoMed.com
Case Of The Month - January, 2003 Image 1 minimal disease. Image 2 19 year old. Image 3 19 tear old patient. Diagnosis Multiple Enchodromatosis (ollier s disease). Discussion http://cases.pedrad.org/case.php?month=January&year=2003
OLLIER'S DISEASE Definition Home/O/OL/ollier S disease. Medical Dictionary Search Engine. Advertise on this site! A service of healthlink-net.com. Browse Dictionary Alphabetically. http://www.books.md/O/dic/Olliersdisease.php
Endochondromatosis, Ollier's Disease, Dyschondroplasia Past Issue Volume 16, Number 4 October 2003, Return to Table of Contents. PDF of this Article. Incidental skeletal abnormalities in a 22year-old man. http://www.baylorhealth.edu/proceedings/16_4/16_4_bufkin.htm