Ollier's Disease - General Practice Notebook medical information from General Practice Notebook. ollier's disease.This is a familial cause of multiple, unilateral chondromata. http://www.gpnotebook.co.uk/cache/-1449525246.htm
Extractions: Francesco Guerreschi, MD, Lecco, ITALY Seventeen limb segments representing eight femora, six tibia and three humeri in nine patients with Ollier's disease were treated using the Ilizarov method. The mean lengthening achieved was 7.0 cm in the femur, 6.8 cm in the tibia and 7.5 cm in the humerus. The average duration of treatment was 7.5 months. Equal limb length was achieved in six of seven lower limbs. Multiplanar angular deformities were corrected in all the limb segments. With a mean follow-up of 4.3 years, the tissue transformation and corrections achieved are observed to be maintained. The corticotomy and tissue manipulation through the sites of the lesions achieved angular correction and lengthening and tissue transformation of the lesions. Moderator(s):Henry J. Mankin, MD, Boston, MA
Ollier's Disease one click For Medical Professionals only. ollier's disease,, Printthis article, (Louis ollier, 18301900, French orthopaedic http://www.amershamhealth.com/medcyclopaedia/Volume VII/OLLIERS DISEASE.asp
Ollier's Disease only one click For Medical Professionals only. ollier's disease,,Print this article, Leopold Louis Xavier Edouard ollier, 1830 http://www.amershamhealth.com/medcyclopaedia/Volume III 1/OLLIERS DISEASE.asp
Foot Problems > Diseases Of The Foot > Ollier's Disease diseases of the foot ollier's disease. ollier's disease is usuallyassociated with a bony prominence under the toenail. Some form http://www.mid-michiganfootandankle.com/prob_diseases_ollier.php
Wheeless' Textbook Of Orthopaedics Main Menu Home Page Multiple Enchodromatosis (ollier's disease). Discussion - originally was described by ollier in late 1800's http://wheeless.orthoweb.be/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 The malignant potential of enchondromatosis Ollier's Disease. An assessment of angular deformity, shortening, and pathological fracture in twenty-one patients.
Health Library - Ollier's Disease SEARCH. ollier's disease. Founded 1985.Mutual support and exchange of ideas forpersons with ollier's or Maffucci's disease, their families and physicians. http://www.muskogeehealth.com/Library/HealthGuide/SelfHelp/topic.asp?hwid=shc29o
Extractions: Received: 13 November 1998 Abstract Among patients with enchondromatosis, those with Ollier's disease are usually considered to be at a lower risk for extra-osseous malignancy than those with Maffucci's disease. However, several reports suggest that Ollier's disease may also be associated with gliomas. We report here the youngest patient in the literature (16 years) to be detected with a brain tumor and Ollier's disease. This is also the first case with diffuse brain stem involvement. Thus, counselling of patients with Ollier's disease may become more difficult than initially thought. Key words Article in PDF format (104 KB) Online publication: May 17, 1999
Abstract Case Report. ollier's disease in association with adjacent fibromatosis. ollier'sdisease (enchondromatosis) is a nonhereditary disorder of mesodermal dysplasia. http://link.springer-ny.com/link/service/journals/00256/contents/02/00483/s00256
Extractions: Khalid Al-Ismail , William C. Torreggiani , Peter L. Munk , John X. O'Connell , Savvakis Nicolaou and Bassam A. Masri Department of Radiology, Vancouver General Hospital, University of British Columbia, 899 West l2th Avenue, Vancouver, BC, Canada V5Z lM9 Department of Pathology, Vancouver General Hospital, University of British Columbia, 899 West l2th Avenue, Vancouver, BC, Canada V5Z lM9 Department of Orthopaedics, Vancouver General Hospital, University of British Columbia, 899 West l2th Avenue, Vancouver, BC, Canada V5Z lM9 Abstract. Ollier's disease (enchondromatosis) is a nonhereditary disorder of mesodermal dysplasia. It is characterized by the presence of multiple enchondromas that typically affect the metaphyseal ends of bones. The association of Ollier's disease with adjacent fibromatosis has, to our knowledge, not been previously described. We report a case of Ollier's disease in association with soft tissue fibromatosis adjacent to the involved upper arm. Key words.
Chondrosarcoma, Secondary To Enchondroma Site The most common precursor is multiple enchondroma or ollier's disease. Thisphenomenon is rare in solitary enchondroma or synovial chondromatosis. http://imc.gsm.com/demos/mskdemo/mspath/enneking/sect14/secencho.html
Extractions: About Table of Contents Malignant Lesions of Bone Help Definition Demographics Clinical Presentation Natural History ... References Chondrosarcoma secondary to enchondroma is a primary neoplasm of cartilaginous histogenesis arising from a pre-existing benign enchondroma. Age: 30 - 50 Site: The most common precursor is multiple enchondroma or Ollier's disease. This phenomenon is rare in solitary enchondroma or synovial chondromatosis. The patient presents with pain at the site of a previously-painless enchondroma. Slow, displacing growth is characteristic of this tumor with very late transition to a high-grade lesion and risk of metastasis. The survival rate is excellent with adequate treatment prior to transition. On radiograph, there is an expanding, radiolucent zone surrounding a calcified enchondroma with endosteal scalloping and periosteal, cortical thickening. [X-Ray] This radiograph shows the original enchondroma at first presentation. The patient was asymptomatic at this time. [X-Ray] This radiograph was made fourteen years later when the patient presented with a secondary chondrosarcoma.
Rockford Register Star Online - Special Reports Amber suffers from ollier's disease, which causes tumors to grow at the jointson the right side of her body and prevents her arm and leg from growing. http://www.rrstar.com/specialreports/amber/index.shtml
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Rockford Register Star Online - Special Reports Eighthgrader at Prairie Hill Elementary School Her disease Amber was diagnosedwith a rare bone disorder called ollier's disease when she was 11 months old. http://www.rrstar.com/specialreports/amber/breakout1.shtml
Extractions: /* You may give each page an identifying name, server, and channel on the next lines. */ var pageName="" var server="" var channel="" var pageType="" var pageValue="" var prop1="News" var prop2="Local_News" var prop3="Special_Reports" var prop4="Julies_Gift" var prop5="" var prop6="news" var prop7="local_news" var prop8="" var prop9="" var prop10="" /********* INSERT THE DOMAIN AND PATH TO YOUR CODE BELOW ************/ /********** DO NOT ALTER ANYTHING ELSE BELOW THIS LINE! *************/ var s_code=' ' Contact Us Subscriptions Advertise About Us ... New Home
Extended Possibilities For Patient With Leg Length Discrepancy Daniel Bowen, a 22year-old resident of League City, Texas, enjoys a normal familylife after growing up with a condition called ollier's disease, which caused http://www.shrinershq.org/shc/houston/olliers1-01.html
Extractions: Home Shrine Shriners Hospitals Hospital Directory ... Archives January 2001 Daniel Bowen, a 22-year-old resident of League City, Texas, enjoys a normal family life after growing up with a condition called Ollier's disease, which caused a significant leg length discrepancy in his right leg. At 5 feet 6 1/2 inches, Daniel Bowen has no problem standing his ground when it comes to his Great Dane, Brutus. After observing him throughout the following day, they realized that Daniel skipped everywhere he went. Daniel's parents and grandparents finally asked him to simply walk across the room, and that's when they noticed that Daniel limped when he walked. After a closer look at his legs, they found that his right leg was shorter then his left leg. "After discovering my lower limb length discrepancy, my parents took me to several doctors before I was finally diagnosed with Ollier's Disease," explained Daniel. Ollier's disease is a non-hereditary congenital defect (present from birth) that causes tumors in the bones of usually just one extremity, affecting not only the long bones, but also those of the foot. The tumors affect the growth plates, which over time causes a lower limb length discrepancy.
Multiple Enchondromatosis: Olliers Disease International Pediatrics. Volume 17, Number 4. Clinical Article. Multiple EnchondromatosisOlliers disease. Neal P. Simon, MD; Michael W. Simon, MD, PhD, FAAP. http://www.int-pediatrics.org/newip/volumes/volume 17/17-4/case/simon.htm
Extractions: International Pediatrics Volume 17, Number 4 Clinical Article Multiple Enchondromatosis: Olliers Disease Neal P. Simon, MD; Michael W. Simon, MD, PhD, FAAP Address reprint requests to Neal P. Simon, MD, 699 West Drive, RR208, Indianapolis, IN 46202. Abstract Multiple enchondromatosis may cause devastating disfigurement and even adversely affect the growth and function of an extremity. Radiographs show typical changes and are generally diagnostic. Surgical intervention is usually warranted and should be sought as soon as the diagnosis is suspected. Approximately 50% of cases of untreated multiple enchondromas undergo malignant sarcomatous transformation. Int Pediatr. 2002;17(4):231-232. Full Article in PDF
Tumors ChondrosarcID5063.txt While most enchondromas are solitary, patients with ollier's disease and Maffucci'ssyndrome demonstrate multiple enchondromas.A minority (15%) of http://www.infobiogen.fr/services/chromcancer/Tumors/chondrosarcID5063.html
Extractions: Figure 2: Corresponding macro-slice showing a lobular architecture, and endosteal cortical thinning. Cytonucle ar appearance can be more readily appreciated in figure 3 Classification Note approximately 90% of chondrosarcomas are histologically of the conventional type; in addition to conventional chondrosarcoma, some rare variants with distinctive microscopic and clinical features are discerned: clear cell chondrosarcoma (1%), mesenchymal chondrosarcoma (2%), juxtacortical chondrosarcoma (2%) and extra-skeletal myxoid chondrosarcoma (5%). Furthermore, dedifferentiated chondrosarcoma is a relatively rare high grade sarcoma next to a low-grade conventional malignant cartilage-forming tumor, comprising 6-10% of all chondrosarcomas. Conventional chondrosarcomas can be categorized according to their location in bone. The majority of chondrosarcomas (75%) are located centrally within the medullary cavity (central chondrosarcoma), a small percentage of which arise within a preexisting benign precursor (enchondroma). While most enchondromas are solitary, patients with Ollier's disease and Maffucci's syndrome demonstrate multiple enchondromas.A minority (15%) of chondrosarcomas develops from the surface of bone (peripheral chondrosarcoma) as a result of malignant transformation within the cartilaginous cap of a solitary or hereditary pre-existent osteochondroma.
IComm: File Not Found! ollier's disease .. ollier's diseaseSelf Help Group http//uhsweb.edu/olliers/olliers.htm. ollier's http://www.icomm.ca/geneinfo/o.htm
