Tumors ChondromaID5147 The chondromas in ollier disease and Maffucci syndrome may demonstrate a greaterdegree of cellularity and cytologic atypia, and may be difficult to http://www.infobiogen.fr/services/chromcancer/Tumors/ChondromaID5147.html
Extractions: Home Genes Leukemias Solid Tumours ... NA Identity Note Chondroma is an uncommon benign tumour which characteristically forms mature cartilage. It is found mostly in the small bones of the hand and/or feet, although it can also occur in long, tubular bones, primarily the humerus, femur and ribs. Occasionally, focal areas of mixoid degeneration may result in a mistaken diagnosis of chondrosarcoma. Classification Chondromas are classified according to their location: enchondroma: within the bone (within the medullary cavity), periosteal chondroma: on the surface of the bone, soft tissue chondroma in the soft tissue. Clinics and Pathology Disease Enchondroma Note Fig: Enchondroma in the distal portion of the femur shaft. (courtesy of Dr Henry DeGroot at http://www.drdegroot.com Enchondroma is usually a solitary benign lesion in intramedullary bone. Usually asymptomatic, it is incidentally discovered as a palpable bony nodule. Rarely, causes soft tissue swelling and pain at the lesion site. Pain can be a sign of pathologic fracture. Both sex are equally affected, and any age group can be involved. It is thought to develop from epiphyseal cartilage rests that subsequently proliferate and slowly enlarge. Approximately 50% of solitary enchondromas are found in the hands, typically in the middle and distal portions of the metacarpals and the proximal portions of the phalanges, 10% in the feet, 20% in the proximal and distal parts of the femur and the proximal part of the humerus.
Extractions: Web resources for "Enchondromatosis" English French German Spanish = Site with HON description - = Site with a robot description info: enter the site: (click below) domain of the site: HONcode - eMedicine - Maffucci Syndrome : Article by Raymond T Kuwahara, MD www.emedicine.com HONcode - NORD - National Organization for Rare Disorders, Inc. www.rarediseases.org II. Congenital and Hereditary Bone Disorders edcenter.med.cornell.edu HONcode - Virtual Children's Hospital: Paediapaedia: Enchondromatosis www.vh.org
List Of Diseases Starting With O: Information From Answers.com List of diseases starting with OA list of diseases in the English wikipedia. Olivopontocerebellar atrophy; ollier disease; Olmsted syndrome http://www.answers.com/topic/list-of-diseases-starting-with-o
Extractions: showHide_TellMeAbout2('false'); Business Entertainment Games Health ... More... On this page: Wikipedia Or search: - The Web - Images - News - Blogs - Shopping List of diseases starting with O Wikipedia List of diseases starting with O A list of diseases in the English wikipedia. A B C D ... N O P Q R S ... Z Ocula Oculo Oculoa-Oculog Oculoauriculofrontonasal syndrome Oculoauriculovertebral dysplasia Oculocerebral hypopigmentation syndrome Cross type Oculocerebral hypopigmentation syndrome type Preus Oculocerebral syndrome with hypopigmentation Oculocerebrocutaneous syndrome Oculocerebrorenal syndrome Oculocutaneous albinism immunodeficiency Oculocutaneous albinism type 1 Oculocutaneous albinism type 2 Oculocutaneous albinism type 3
Enchondromatosis ollier disease. Osteochondromatosis ollier disease Enchondromatosis (Ollier sdisease) of phalanges of fingers Enchondromatosis of great toe and http://www.gfmer.ch/genetic_diseases_v2/gendis_detail_list.php?offset=15&cat3=10
EMedicine Multiple enchondromas in the hand are characteristic of ollier disease or Maffucci ollier disease is a rare bone disorder characterized by multiple http://master.emedicine.com/email/radio/radio72/radio72answer.html
Extractions: Ollier disease: The hand radiograph reveals multiple, well-defined, and centrally located round and oval lytic lesions with endosteal scalloping, sclerotic margins, and expansion of the cortex in the metacarpal, middle phalanx, and distal phalanx bones of the left hand. The lesions have a characteristic rings-and-arcs pattern of calcification, which suggests cartilaginous tumors. No pathologic fracture of any of these lesions is seen. The lesions are consistent with enchondromas. Multiple enchondromas in the hand are characteristic of Ollier disease or Maffucci syndrome. The differential diagnosis for a single lesion with this characteristic appearance includes epidermoid inclusion cyst, unicameral bone cyst, giant cell tumor, fibrous dysplasia, bone infarct, and chondrosarcoma. Ollier disease is a rare bone disorder characterized by multiple enchondromas of the metaphyses and diaphyses of the bones of the extremities. The disease may be present at birth, but patients usually present in early childhood, when symptoms, such as deformities or improper limb growth, become apparent. The disease primarily affects one side of the body and typically only the long bones of the extremities. Maffucci syndrome is Ollier disease plus multiple soft-tissue cavernous hemangiomas. These hemangiomas usually appear after puberty as multiple nodules, typically in the digits and extremities. On radiographs, they are characterized by soft tissue masses with internal phleboliths.
Advances In Anatomic Pathology - UserLogin of ollier disease and Maffucci syndrome, multiple hereditary exostoses, one other example arising in the finger of a patient with ollier disease. http://www.anatomicpathology.com/pt/re/aapath/fulltext.00125480-200209000-00005.
Extractions: Disease/Genetic Disorder Tissue affected Gene General Information Molecular Information References Acrocapitofemoral Dysplasia (ACFD) skeletal ihh OMIM Hellemans et. al. (2003) Am. J. Hum. Genet. 72: 1040-1046 Brachydactyly,Type A1 (BDA1) Limbs ihh OMIM Gao et. al. (2001) Nature Genet. 28: 386-388 Breast Cancer Breast National Cancer Institute OMIM Kubo M. et.al. (2004) Cancer Res. 64:6071-6074 Coloboma,Ocular Eye shh OMIM Schimmenti et. al. (2003) Am. J. Med. Genet. 116: 215-221, Desmosterolosis shh,ihh,dhh OMIM Enchondromatosis, Multiple Maffucci Syndrome Bone OMIM Hopyan et al. (2002) Nat Genet. 30:306-10 OMIM OMIM OMIM Esophageal Cancer Esophagus National Cancer Institute OMIM Watkins and Peacock (2004) Biochem Pharmacol. 68:1055-60
Diagnostic Molecular Pathology - UserLogin Patient has ollier disease.Patient has hereditary multiple exostoses syndrome . The chondrosarcomas from two patients with ollier disease in the present http://www.molecularpathology.com/pt/re/dmp/fulltext.00019606-200112000-00004.ht
Penn State Faculty Research Expertise Database (FRED) Maffucci Syndrome, Ollier s Disease. ollier disease, Disease, Ollier. Disease,Ollier s, Enchondromas, Multiple. Enchondromatoses, Enchondroses, Multiple http://fred.hmc.psu.edu/ds/retrieve/fred/meshdescriptor/D004687
Ollier's Disease ollier s disease is a condition of multiple enchondromas. Patients with ollier sdisease need to have their condition closely monitored because of the risk http://orthopedics.about.com/cs/tumors/g/olliers.htm
Extractions: var zLb=1; var zIoa1 = new Array('Related Words','Enchondroma','http://orthopedics.about.com/library/glossary/bldef-enchondroma.htm','Cartilage','http://orthopedics.about.com/library/glossary/bldef-cartilage.htm','Benign','http://orthopedics.about.com/cs/tumors/g/benign.htm'); zJs=10 zJs=11 zJs=12 zJs=13 zc(5,'jsc',zJs,9999999,'') zfs=0;zCMt='a67' About Orthopedics Orthopedics Essentials ... Help zau(256,140,140,'el','http://z.about.com/0/ip/417/C.htm','');w(xb+xb+' ');zau(256,140,140,'von','http://z.about.com/0/ip/496/6.htm','');w(xb+xb); Sign Up Now for the Orthopedics newsletter!
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. This site contains general information only and does not constitute specific advice. AAMED
AAMED: American Association Of Multiple Enchondroma Diseases We are often asked if ollier s disease or Maffucci s syndrome are hereditary Living with olliers disease or Maffuccis syndrome can be a fine balancing http://www.aamed.net/modules.php?name=News&file=categories&op=newindex&catid=4
Birth Disorder Information Directory - O ollier s disease (Dyschondroplasia, Multiple Enchodromatosis, Osteochondromatosis) See ollier s disease. Osteodysgenesis. Multisynostotic http://www.bdid.com/defecto.htm
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.
Core Curriculum - POSNA Describe the clinical and radiographic features of ollier s disease ollier s disease is an uncommon condition of multiple enchondromatosis. http://www.posna.org/index?service=page/coreCurriculum&article=olliersDisease.ht
Multiple Enchondroma Diseases / Family Village Maffucci Syndrome from eMedicine ollier s disease About Enchondroma diseases Dyschondroplasia ollier s disease and Maffucci s disease http://www.familyvillage.wisc.edu/Lib_olli.htm
Extractions: Web: http://www.aamed.net/ 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. American Association of Multiple Enchondroma Diseases Discussion Boards
