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Enchondromatosis |
Classification and external resources |
Specialty |
medical genetics |
ICD-10 |
Q78.4 |
ICD-9-CM |
756.4 |
DiseasesDB |
9212 |
eMedicine |
radio/247 |
MeSH |
D004687 |
[edit on Wikidata]
|
Enchondromatosis is a form of osteochondrodysplasia characterized by a proliferation of enchondromas.
Ollier disease can be considered a synonym for enchondromatosis.[1] Maffucci syndrome is enchondromatosis with hemangiomatosis.[2]
References
- ^ "Ollier disease" at Dorland's Medical Dictionary
- ^ Faik A, Allali F, El Hassani S, Hajjaj-Hassouni N (February 2006). "Maffucci's syndrome: a case report". Clin. Rheumatol. 25 (1): 88–91. PMID 16234991. doi:10.1007/s10067-005-1101-1.
Tumours of bone and cartilage (ICD-O 9180–9269) (C40–C41/D16, 170/213)
|
Diaphysis |
Myeloid |
|
Epithelial |
|
PNET/Ewing family |
|
|
Metaphysis |
Osteoblast |
- Osteoid osteoma
- Osteoblastoma
- Osteoma/osteosarcoma
|
Chondroblast |
- Chondroma/ecchondroma/enchondroma
- Enchondromatosis
- Extraskeletal chondroma
- Chondrosarcoma
- Mesenchymal chondrosarcoma
- Myxoid chondrosarcoma
- Osteochondroma
- Chondromyxoid fibroma
|
Fibrous |
- (Peripheral) Ossifying fibroma
- Fibrosarcoma
|
|
Epiphysis |
|
Other/ungrouped |
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Osteochondrodysplasia (Q77–Q78, 756.4–756.5)
|
Osteodysplasia//
osteodystrophy |
Diaphysis |
- Camurati–Engelmann disease
|
Metaphysis |
- Metaphyseal dysplasia
- Jansen's metaphyseal chondrodysplasia
- Schmid metaphyseal chondrodysplasia
|
Epiphysis |
- Spondyloepiphyseal dysplasia congenita
- Multiple epiphyseal dysplasia
- Otospondylomegaepiphyseal dysplasia
|
Osteosclerosis |
- Raine syndrome
- Osteopoikilosis
- Osteopetrosis
|
Other/ungrouped |
- FLNB
- Opsismodysplasia
- Polyostotic fibrous dysplasia
|
|
Chondrodysplasia/
chondrodystrophy
(including dwarfism) |
Osteochondroma |
- osteochondromatosis
- Hereditary multiple exostoses
|
Chondroma/enchondroma |
- enchondromatosis
- Ollier disease
- Maffucci syndrome
|
Growth factor receptor |
FGFR2: |
|
FGFR3: |
- Achondroplasia
- Thanatophoric dysplasia
|
|
COL2A1 collagen disease |
- Achondrogenesis
- Hypochondrogenesis
|
SLC26A2 sulfation defect |
- Achondrogenesis
- Autosomal recessive multiple epiphyseal dysplasia
- Atelosteogenesis, type II
- Diastrophic dysplasia
|
Chondrodysplasia punctata |
- Rhizomelic chondrodysplasia punctata
- Conradi–Hünermann syndrome
|
Other dwarfism |
- Fibrochondrogenesis
- Short rib – polydactyly syndrome
- Majewski's polydactyly syndrome
- Léri–Weill dyschondrosteosis
|
|
UpToDate Contents
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English Journal
- [Multiple enchondromatosis, Ollier disease].
- Tejada Gallego J1, Martinez-Gonzalez C2.
- Anales de pediatria (Barcelona, Spain : 2003).An Pediatr (Barc).2016 Jun 7. pii: S1695-4033(16)30179-5. doi: 10.1016/j.anpedi.2016.04.011. [Epub ahead of print]
- PMID 27288070
- Frederik Ruysch (1638-1731): Historical perspective and contemporary analysis of his teratological legacy.
- Boer L1, Radziun AB2, Oostra RJ3.
- American journal of medical genetics. Part A.Am J Med Genet A.2016 Apr 29. doi: 10.1002/ajmg.a.37663. [Epub ahead of print]
- The Peter the Great Museum of Anthropology and Ethnography (Kunstkamera) in Saint Petersburg is the oldest museum in Russia. It keeps the remains of the anatomical collection of the world-famous 17th century Dutch anatomist Frederik Ruysch. This unique collection was bought and shipped in 1717 by Cz
- PMID 27126916
- Characteristics of gliomas in patients with somatic IDH mosaicism.
- Bonnet C1,2,3, Thomas L1, Psimaras D4, Bielle F5,6,7,8, Vauléon E9, Loiseau H10, Cartalat-Carel S1, Meyronet D2,3,11, Dehais C3, Honnorat J1,2,12, Sanson M4,6,7,8, Ducray F13,14,15.
- Acta neuropathologica communications.Acta Neuropathol Commun.2016 Mar 31;4:31. doi: 10.1186/s40478-016-0302-y.
- IDH mutations are found in the majority of adult, diffuse, low-grade and anaplastic gliomas and are also frequently found in cartilaginous tumors. Ollier disease and Maffucci syndrome are two enchondromatosis syndromes characterized by the development of multiple benign cartilaginous tumors due to p
- PMID 27036230
Japanese Journal
- 創外固定法で前腕変形矯正を行った enchondromatosis の1例
- 創外固定法で前腕変形矯正を行ったenchondromatosisの1例
Related Links
- Enchondromatosis, also known as Ollier disease, is a non-hereditary, sporadic, skeletal disorder characterised by multiple enchondromas that are principally located in the metaphyseal regions. Terminology Some authors make a ...
- Looking for online definition of enchondromatosis in the Medical Dictionary? enchondromatosis explanation free. What is enchondromatosis? Meaning of enchondromatosis medical term. What does enchondromatosis mean? ? ...
Related Pictures
![multiple enchondromatosis](https://1mg.info/0/m/5/2188.jpg)
![multiple enchondromatosis](https://1mg.info/0/m/5/2184.jpg)
![Enchondromatosis; Ollier's Disease; Maffucci Syndrome; Enchondroma, Multiple](https://1mg.info/0/q/2/1887.jpg)
![Enchondromatosis; Ollier's Disease; Maffucci Syndrome; Enchondroma, Multiple](https://1mg.info/0/k/c/0249.jpg)
![Enchondromatosis; Ollier's Disease; Maffucci Syndrome; Enchondroma, Multiple](https://1mg.info/0/q/2/1888.jpg)
![Hard tissue practical final - Radiography Idk with Orndorff at Sherman College of](https://1mg.info/0/m/5/2186.jpg)
![Enchondromatosis or Ollier Disease | Bone and Spine](https://1mg.info/0/q/2/1889.jpg)
★リンクテーブル★
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オリエ病、Ollier病
- 関
- enchondromatosis
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- 関
- enchondromatosis
- 関
- enchondromatosis