類腱線維腫
WordNet
- nonmalignant tumor of connective tissue
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2014/04/25 06:49:40」(JST)
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Desmoplastic fibroma |
Classification and external resources |
ICD-O: |
M8823/1 |
DiseasesDB |
32871 |
MeSH |
D018220 |
In medicine, a desmoplastic fibroma is a benign fibrous tumor of bone, affecting children and young adults, potentially resulting in cortical bone destruction.[1]
It can also occur in the hand.[2]
A famous occurrence of this particular form of the disease involved Italo-Australian Riccardo Torresan in 2011, with 18 cm of femur needing to be removed with the now widely recognized method of "aggressive curettage" being employed.[3]
References
- ^ Mondofacto online medical dictionary - definition of desmoplastic fibroma 05 Mar 2000
- ^ Bernstein ML, Chung KC (October 2008). "Desmoplastic fibroma of the hand: case report". J Hand Surg [Am] 33 (8): 1405–8. doi:10.1016/j.jhsa.2008.03.005. PMID 18929210.
- ^ http://www.bonetumor.org/tumors-fibrous-tissue/desmoplastic-fibroma
Connective/soft tissue tumors and sarcomas (ICD-O 8800–9059) (C45–C49/D17–D21, 171/214–215)
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Not otherwise specified (8800–8809) |
- Soft-tissue sarcoma
- Desmoplastic small-round-cell tumor
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Connective tissue neoplasm |
Fibromatous (8810–8839) |
Fibroma/fibrosarcoma: |
- Dermatofibrosarcoma protuberans
- Desmoplastic fibroma
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Fibroma/fibromatosis: |
- Aggressive infantile fibromatosis
- Aponeurotic fibroma
- Collagenous fibroma
- Diffuse infantile fibromatosis
- Familial myxovascular fibromas
- Fibroma of tendon sheath
- Fibromatosis colli
- Infantile digital fibromatosis
- Juvenile hyaline fibromatosis
- Plantar fibromatosis
- Pleomorphic fibroma
- Oral submucous fibrosis
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Histiocytoma/histiocytic sarcoma: |
- Benign fibrous histiocytoma
- Malignant fibrous histiocytoma
- Atypical fibroxanthoma
- Solitary fibrous tumor
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Myxomatous (8840–8849) |
- Myxoma/myxosarcoma
- Cutaneous myxoma
- Superficial acral fibromyxoma
- Angiomyxoma
- Ossifying fibromyxoid tumour
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Fibroepithelial (9000–9039) |
- Brenner tumour
- Fibroadenoma
- Phyllodes tumor
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Synovial-like (9040–9049) |
- Synovial sarcoma
- Clear-cell sarcoma
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Lipomatous (8850–8889) |
- Lipoma/liposarcoma
- Myelolipoma
- Myxoid liposarcoma
- PEComa
- Chondroid lipoma
- Intradermal spindle cell lipoma
- Pleomorphic lipoma
- Lipoblastomatosis
- Spindle cell lipoma
- Hibernoma
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Myomatous (8890–8929) |
general: |
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smooth muscle: |
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skeletal muscle: |
- Rhabdomyoma/rhabdomyosarcoma: Embryonal rhabdomyosarcoma
- Alveolar rhabdomyosarcoma
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- Leiomyoma
- Angioleiomyoma
- Angiolipoleiomyoma
- Genital leiomyoma
- Leiomyosarcoma
- Multiple cutaneous and uterine leiomyomatosis syndrome
- Multiple cutaneous leiomyoma
- Neural fibrolipoma
- Solitary cutaneous leiomyoma
- STUMP
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Complex mixed and stromal (8930–8999) |
- Adenomyoma
- Pleomorphic adenoma
- Mixed Müllerian tumor
- Mesoblastic nephroma
- Wilms' tumor
- Malignant rhabdoid tumour
- Clear-cell sarcoma of the kidney
- Hepatoblastoma
- Pancreatoblastoma
- Carcinosarcoma
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Mesothelial (9050–9059) |
- Mesothelioma
- Adenomatoid tumor
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see also Template:Connective tissue
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anat (h/n, u, t/d, a/p, l)/phys/devp/hist
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noco (m, s, c)/cong (d)/tumr, sysi/epon, injr
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UpToDate Contents
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English Journal
- [Value of MDM2, CDK4 and SATB2 immunohistochemistry in histologic diagnosis of low-grade osteosarcoma].
- Chen CY1, Zhang HZ, Jiang ZM, Zhou J, Chen J, Liu L.
- Zhonghua bing li xue za zhi Chinese journal of pathology.Zhonghua Bing Li Xue Za Zhi.2016 Jun 8;45(6):387-92. doi: 10.3760/cma.j.issn.0529-5807.2016.06.007.
- OBJECTIVE: To investigate the value of combined application of MDM2, CDK4 and SATB2 immunohistochemistry in pathological diagnosis of low-grade osteosarcoma.METHODS: Forty-seven cases of low grade osteosarcoma, including low grade central osteosarcoma (n=20) and parosteal osteosarcoma (n=27), were s
- PMID 27256046
- Myofibroblastoma of the mandible in a 3-year-old child.
- Hajeri S1, Al Jabab A2, Al Sheddi M3, Fatani H2.
- Oral and maxillofacial surgery.Oral Maxillofac Surg.2016 Mar;20(1):103-7. doi: 10.1007/s10006-015-0524-3. Epub 2015 Aug 19.
- Myofibroblastoma is a rare benign tumor of the head and neck region, which is characterized by a large, rapidly growing, and destructive mass. A 3-year-old boy presented with an 8-week history of a rapidly growing swelling of the right mandible. Examination revealed a firm 13-cm mass occupying the e
- PMID 26282517
- Desmoplastic Fibroma of the Pediatric Cranium: An Aggressive Skull Tumor with Local Recurrence.
- Koiso T1, Muroi A, Yamamoto T, Sakamoto N, Matsumura A.
- Neurologia medico-chirurgica.Neurol Med Chir (Tokyo).2016 Feb 15;56(2):85-8. doi: 10.2176/nmc.cr.2015-0167. Epub 2016 Jan 22.
- Cranial desmoplastic fibroma (DF) is extremely rare and only 20 cases, including only 7 pediatric cases, have been reported previously. We describe the first case of a child with cranial DF that increased in size over a short-term and recurred after resection. The aim of this case report was to disc
- PMID 26804188
Japanese Journal
- 症例 高齢者に発生した下顎骨類腱線維腫(desmoplastic fibroma)の1例
Related Links
- The diagnosis of desmoplastic fibroma is difficult to make radiologically. Plain xray shows an osteolytic, expansile, medullary lesion with well defined sclerotic margins. The oval tumor is often found in the metaphysis aligned with the ...
- Desmoplastic fibromas (DF) are extremely rare bone tumours that do not metastasize, but may be locally aggressive. They are considered to be a bony counterpart of soft tissue desmoid tumours and are histologically identical.
Related Pictures
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- 関
- fibrogenic