WordNet
- abnormal hardening or eburnation of bone
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2015/02/16 22:11:03」(JST)
[Wiki en表示]
| Osteosclerosis |
| Classification and external resources |
| ICD-10 |
M85.8, Q77.4 |
| ICD-9 |
756.52 |
| DiseasesDB |
15823 |
| NCI |
Osteosclerosis |
| MeSH |
D010026 |
Osteosclerosis, an elevation in bone density,[1] is normally detected on a radiograph as an area of increased opacity; that is, where more mineral is present in the bone to absorb or deflect the X-ray beam. Localized osteosclerosis can be caused by injuries that compress the bone, by osteoarthritis, and osteoma.
It is associated with:
- Melorheostosis
- Osteopetrosis
- Osteopoikilosis
- Chronic idiopathic myelofibrosis
- Skeletal fluorosis
It can also be associated with Hepatitis C.[2]
References
- ^ "Medcyclopaedia - Osteosclerosis". Archived from the original on 2012-02-05. Retrieved 2007-12-23.
- ^ Fiore CE, Riccobene S, Mangiafico R, Santoro F, Pennisi P (2005). "Hepatitis C-associated osteosclerosis (HCAO): report of a new case with involvement of the OPG/RANKL system". Osteoporos Int 16 (12): 2180–4. doi:10.1007/s00198-005-1858-8. PMID 15983730.
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Osteochondropathy (M80–M94, 730–733)
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| Osteopathies |
| Osteitis |
| endocrine bone disease: |
|
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| infectious bone disease: |
- Osteomyelitis
- Sesamoiditis
- Brodie abscess
- Periostitis
- Vertebral osteomyelitis
|
|
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Bone density
and structure |
| Density / metabolic bone disease |
- Osteoporosis
- Osteopenia
- Osteomalacia
|
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| Continuity of bone |
- Pseudarthrosis
- Stress fracture
|
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| Other |
- Fibrous dysplasia
- Skeletal fluorosis
- bone cyst
- Hyperostosis
- Infantile cortical hyperostosis
- Osteosclerosis
- Pycnodysostosis
|
|
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| Bone resorption |
- Osteolysis
- Hajdu-Cheney syndrome
- Ainhum
|
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| Ischemia |
|
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| Other |
- Paget's disease of bone
- Algoneurodystrophy
- Hypertrophic pulmonary osteoarthropathy
- Nonossifying fibroma
|
|
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| Chondropathies |
|
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| Both |
| Osteochondritis |
- Osteochondritis dissecans
|
|
| Juvenile osteochondrosis |
| leg: |
- hip
- Legg–Calvé–Perthes syndrome
- tibia
- Osgood-Schlatter disease
- Blount's disease
- foot
- Köhler disease
- Sever's disease
|
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| spine |
|
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| arm: |
|
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Index of bones and cartilage
|
|
| Description |
- Anatomy
- skull
- face
- neurocranium
- compound structures
- foramina
- upper extremity
- torso
- pelvis
- lower extremity
- Physiology
- Development
- Cells
|
|
| Disease |
- Congenital
- Neoplasms and cancer
- Fracture
- Other
- Symptoms and signs
|
|
| Treatment |
|
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|
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Osteochondrodysplasia (Q77–Q78, 756.4–756.5)
|
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Osteodysplasia//
osteodystrophy |
| Diaphysis |
- Camurati–Engelmann disease
|
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| Metaphysis |
- Metaphyseal dysplasia
- Jansen's metaphyseal chondrodysplasia
- Schmid metaphyseal chondrodysplasia
|
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| Epiphysis |
- Spondyloepiphyseal dysplasia congenita
- Multiple epiphyseal dysplasia
- Otospondylomegaepiphyseal dysplasia
|
|
| Osteosclerosis |
- Raine syndrome
- Osteopoikilosis
- Osteopetrosis
|
|
| Other/ungrouped |
- FLNB
- Opsismodysplasia
- Polyostotic fibrous dysplasia
|
|
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Chondrodysplasia/
chondrodystrophy
(including dwarfism) |
| Osteochondroma |
- osteochondromatosis
- Hereditary multiple exostoses
|
|
| Chondroma/enchondroma |
- enchondromatosis
- Ollier disease
- Maffucci syndrome
|
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| Growth factor receptor |
| FGFR2: |
|
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| FGFR3: |
- Achondroplasia
- Thanatophoric dysplasia
|
|
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| 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
|
|
|
Index of bones and cartilage
|
|
| Description |
- Anatomy
- skull
- face
- neurocranium
- compound structures
- foramina
- upper extremity
- torso
- pelvis
- lower extremity
- Physiology
- Development
- Cells
|
|
| Disease |
- Congenital
- Neoplasms and cancer
- Fracture
- Other
- Symptoms and signs
|
|
| Treatment |
|
|
|
UpToDate Contents
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English Journal
- Bone mineral density, bone turnover markers and fractures in patients with indolent systemic mastocytosis.
- Rossini M, Zanotti R, Bonadonna P, Artuso A, Caruso B, Schena D, Vecchiato D, Bonifacio M, Viapiana O, Gatti D, Senna G, Riccio A, Passalacqua G, Pizzolo G, Adami S.SourceRheumatology Section, Department of Medicine, University of Verona, Italy; Multidisciplinary Mastocytosis Outpatient Clinic, Azienda Ospedaliera Universitaria Integrata of Verona, Italy.
- Bone.Bone.2011 Oct;49(4):880-5. Epub 2011 Jul 14.
- OBJECTIVE: We systematically assessed bone mineral density (BMD), bone turnover markers (BTM), and fractures in a large cohort of patients with Indolent Systemic Mastocytosis (ISM).METHODS: Eighty-two patients (mean age 48years, 37 women) with ISM were studied. BMD was measured by dual X-ray absorpt
- PMID 21782049
- Erdheim-Chester disease with multisystem involvement in a 4-year-old.
- Song SY, Lee SW, Ryu KH, Sung SH.SourceDepartment of Radiology, Ewha Womans University School of Medicine, Seoul, South Korea, littlessook@hanmail.net.
- Pediatric radiology.Pediatr Radiol.2011 Aug 31. [Epub ahead of print]
- Erdheim-Chester disease is a rare form of non-Langerhans histiocytosis of unknown origin occurring mainly in adults. It is extremely rare in children. We report a case of a 4-year-old boy with Erdheim-Chester disease that initially presented as hemifacial palsy and bone pain with multisystem involve
- PMID 21879308
Japanese Journal
- Progressive osteosclerosis and visceral calcification after cord blood transplantation
- ASADA Noboru,ISHII Shinichi,WAKAHASHI Kanako,KAWANO Hiroki,KAWAMORI Yuriko,NISHIKAWA Shinichiro,MINAGAWA Kentaro,OKAMURA Atsuo,SHIMOYAMA Manabu,KATAYAMA Yoshio,HAYASHI Yoshitake,ITOH Tomoo,TANIMOTO Mitsune,MATSUI Toshimitsu
- International journal of hematology 91(3), 542-545, 2010-04-15
- NAID 10026401555
- Idiopathic osteosclerosis in the mandible associated with abnormal tooth root formation
- OSHIMA Shohei,SUZUKI Junichi,YAWAKA Yasutaka
- Pediatric dental journal : international journal of Japanese Society of Pediatric Dentistry 20(1), 91-94, 2010-03-31
- NAID 10027485666
Related Links
- Osteosclerosis, an elevation in bone density, is normally detected on an X-ray as an area of whiteness, and is where the bone density has significantly increased. Localized osteosclerosis can be caused by injuries that compress the bone, by ...
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