胞巣状横紋筋肉腫、胞巣型横紋筋肉腫
WordNet
- pertaining to the tiny air sacs of the lungs
- pertaining to the sockets of the teeth or that part of the upper jaw; "alveolar processes"
- a highly malignant neoplasm derived from striated muscle (同)rhabdosarcoma
PrepTutorEJDIC
- 歯茎音の(舌先を上歯茎にふれて発音する) / 肺胞の;歯槽(しそう)の / 歯茎音
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2014/08/12 19:57:41」(JST)
[Wiki en表示]
Alveolar rhabdomyosarcoma |
Classification and external resources |
ICD-O: |
M8920/3 |
MeSH |
D018232 |
Alveolar rhabdomyosarcoma is a type of rhabdomyosarcoma characterized by its appearance, which is similar to the alveoli of the lungs.
It can be associated with a fusion protein between PAX3 and FKHR (now known as FOXO1).[1][2]
It can also be associated with PAX7-FKHR.[3][4]
References
- ^ Fredericks WJ, Galili N, Mukhopadhyay S, et al. (March 1995). "The PAX3-FKHR fusion protein created by the t(2;13) translocation in alveolar rhabdomyosarcomas is a more potent transcriptional activator than PAX3". Mol. Cell. Biol. 15 (3): 1522–35. PMC 230376. PMID 7862145.
- ^ Mercado GE, Xia SJ, Zhang C, et al. (June 2008). "Identification of PAX3-FKHR-regulated genes differentially expressed between alveolar and embryonal rhabdomyosarcoma: focus on MYCN as a biologically relevant target". Genes Chromosomes Cancer 47 (6): 510–20. doi:10.1002/gcc.20554. PMID 18335505.
- ^ Mercado GE, Barr FG (February 2007). "Fusions involving PAX and FOX genes in the molecular pathogenesis of alveolar rhabdomyosarcoma: recent advances". Curr. Mol. Med. 7 (1): 47–61. doi:10.2174/156652407779940440. PMID 17311532.
- ^ Laé M, Ahn EH, Mercado GE, et al. (June 2007). "Global gene expression profiling of PAX-FKHR fusion-positive alveolar and PAX-FKHR fusion-negative embryonal rhabdomyosarcomas". J. Pathol. 212 (2): 143–51. doi:10.1002/path.2170. PMID 17471488.
See also
Connective/soft tissue tumors and sarcomas (ICD-O 8800–9059) (C45–C49/D17–D21, 171/214–215)
|
|
Not otherwise specified (8800–8809) |
- Soft-tissue sarcoma
- Desmoplastic small-round-cell tumor
|
|
Connective tissue neoplasm |
Fibromatous (8810–8839) |
Fibroma/fibrosarcoma: |
- Dermatofibrosarcoma protuberans
- Desmoplastic fibroma
|
|
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
|
|
Histiocytoma/histiocytic sarcoma: |
- Benign fibrous histiocytoma
- Malignant fibrous histiocytoma
- Atypical fibroxanthoma
- Solitary fibrous tumor
|
|
|
Myxomatous (8840–8849) |
- Myxoma/myxosarcoma
- Cutaneous myxoma
- Superficial acral fibromyxoma
- Angiomyxoma
- Ossifying fibromyxoid tumour
|
|
Fibroepithelial (9000–9039) |
- Brenner tumour
- Fibroadenoma
- Phyllodes tumor
|
|
Synovial-like (9040–9049) |
- Synovial sarcoma
- Clear-cell sarcoma
|
|
|
Lipomatous (8850–8889) |
- Lipoma/liposarcoma
- Myelolipoma
- Myxoid liposarcoma
- PEComa
- Chondroid lipoma
- Intradermal spindle cell lipoma
- Pleomorphic lipoma
- Lipoblastomatosis
- Spindle cell lipoma
- Hibernoma
|
|
Myomatous (8890–8929) |
general: |
|
|
smooth muscle: |
|
|
skeletal muscle: |
- Rhabdomyoma/rhabdomyosarcoma: Embryonal rhabdomyosarcoma
- Alveolar rhabdomyosarcoma
|
|
- Leiomyoma
- Angioleiomyoma
- Angiolipoleiomyoma
- Genital leiomyoma
- Leiomyosarcoma
- Multiple cutaneous and uterine leiomyomatosis syndrome
- Multiple cutaneous leiomyoma
- Neural fibrolipoma
- Solitary cutaneous leiomyoma
- STUMP
|
|
|
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
|
|
Mesothelial (9050–9059) |
- Mesothelioma
- Adenomatoid tumor
|
|
see also Template:Connective tissue
|
anat (h/n, u, t/d, a/p, l)/phys/devp/hist
|
noco (m, s, c)/cong (d)/tumr, sysi/epon, injr
|
|
|
|
|
Pathology: chromosome abnormalities (Q90–Q99, 758)
|
|
Autosomal |
Trisomies |
- Down syndrome
- Edwards syndrome
- Patau syndrome
- Trisomy 9
- Warkany syndrome 2
- Cat eye syndrome/Trisomy 22
- Trisomy 16
|
|
Monosomies/deletions |
- 1q21.1 deletion syndrome/1q21.1 duplication syndrome/TAR syndrome
- Wolf–Hirschhorn syndrome
- Cri du chat/Chromosome 5q deletion syndrome
- Williams syndrome
- Jacobsen syndrome
- Miller–Dieker syndrome/Smith–Magenis syndrome
- DiGeorge syndrome
- 22q11.2 distal deletion syndrome
- 22q13 deletion syndrome
- genomic imprinting
- Angelman syndrome/Prader–Willi syndrome (15)
- Distal 18q-/Proximal 18q-
|
|
|
X/Y linked |
Monosomy |
|
|
Trisomy/tetrasomy,
other karyotypes/mosaics |
- Klinefelter syndrome (47,XXY)
- 48,XXYY
- 48,XXXY
- 49,XXXYY
- 49,XXXXY
- Triple X syndrome (47,XXX)
- 48,XXXX
- 49,XXXXX
|
|
|
Translocations |
Leukemia/lymphoma |
Lymphoid |
- Burkitt's lymphoma t(8 MYC;14 IGH)
- Follicular lymphoma t(14 IGH;18 BCL2)
- Mantle cell lymphoma/Multiple myeloma t(11 CCND1:14 IGH)
- Anaplastic large cell lymphoma t(2 ALK;5 NPM1)
- Acute lymphoblastic leukemia
|
|
Myeloid |
- Philadelphia chromosome t(9 ABL; 22 BCR)
- Acute myeloblastic leukemia with maturation t(8 RUNX1T1;21 RUNX1)
- Acute promyelocytic leukemia t(15 PML,17 RARA)
- Acute megakaryoblastic leukemia t(1 RBM15;22 MKL1)
|
|
|
Other |
- Ewing's sarcoma t(11 FLI1; 22 EWS)
- Synovial sarcoma t(x SYT;18 SSX)
- Dermatofibrosarcoma protuberans t(17 COL1A1;22 PDGFB)
- Myxoid liposarcoma t(12 DDIT3; 16 FUS)
- Desmoplastic small round cell tumor t(11 WT1; 22 EWS)
- Alveolar rhabdomyosarcoma t(2 PAX3; 13 FOXO1) t (1 PAX7; 13 FOXO1)
|
|
|
Other |
- Fragile X syndrome
- Uniparental disomy
- XX male syndrome
- Ring chromosome (13; 14; 15; 20)
|
|
UpToDate Contents
全文を閲覧するには購読必要です。 To read the full text you will need to subscribe.
English Journal
- Pediatric rhabdomyosarcoma at presentation: Can cross-sectional imaging findings predict pathologic tumor subtype?
- Franco A, Lewis KN, Lee JR.SourceGeorgia Health Sciences University, Children's Medical Center, Department of Radiology, 1120 15th Avenue, Augusta, GA 30912, United States.
- European journal of radiology.Eur J Radiol.2011 Dec;80(3):e446-50. Epub 2011 Feb 8.
- OBJECTIVE: The purpose of the study is to determine whether there are cross-sectional imaging features of pediatric rhabdomyosarcoma that are specific to the different pathologic subtypes of the tumor.MATERIALS AND METHODS: Medical records of 14 pediatric patients who were diagnosed with rhabdomyosa
- PMID 21306853
- Soft tissue sarcoma across the age spectrum: a population-based study from the Surveillance Epidemiology and End Results database.
- Ferrari A, Sultan I, Huang TT, Rodriguez-Galindo C, Shehadeh A, Meazza C, Ness KK, Casanova M, Spunt SL.SourcePediatric Oncology Unit, Istituto Nazionale Tumori, Milano, Italy.
- Pediatric blood & cancer.Pediatr Blood Cancer.2011 Dec 1;57(6):943-9. doi: 10.1002/pbc.23252. Epub 2011 Jul 25.
- BACKGROUND: Soft tissue sarcomas (STS) are a heterogeneous group of mesenchymal malignancies that occur throughout the lifespan. The impact of age on disease features and outcome is unclear.METHODS: We analyzed the clinical features and outcome of all STS cases registered between 1973 and 2006 in th
- PMID 21793180
Japanese Journal
- 荒 志保子,坪田 大,郷 充 [他],新谷 朋子,才川 悦子,長屋 朋典,永井 洋輔,関 伸彦,氷見 徹夫
- 耳鼻咽喉科臨床 104(5), 325-330, 2011-05-01
- … Although the most common soft-tissue sarcoma in children, rhabdomyosarcoma (RMS) is rare in adults. … Tumor biopsy showed alveolar rhabdosarcoma. …
- NAID 10027972572
- Aggressive Spindle Cell Rhabdomyosarcoma in an 11-Month-Old Boxer Dog
- Roza Marcello Rodrigues da,Amorim Rivadavio Fernandes Batista de,Carneiro Fabiana Pirani [他],BENATTO Nara,BARRIVIERA Mauricio,MIGUEL Márcia Cristina da Costa
- 日本獣醫學会会誌 72(10), 1363-1366, 2010
- … Rhabdomyosarcoma (RMS) is a malignant neoplasm derived from mesenchymal tissue with a tendency toward myogenic differentiation associated with the embryogenesis of skeletal muscle. … According to the histological features, it can be classified in embryonal, botryoid, alveolar, and pleomorphic, which usually correspond to clinical behavior and prognosis. …
- NAID 130000264213
- Alveolar Rhabdomyosarcoma Mimicking Nasal Lymphoma at The Initial Presentation
- IHARA Tatsuya,OKAMURA Daisuke,TAKAHASHI Naoki,KOHRI Mika,KAYANO Hidekazu,TAMARU Jun-ichi,NIITSU Nozomi
- Journal of clinical and experimental hematopathology 48(2), 61-64, 2008-11-01
- … Rhabdomyosarcoma is exceedingly rare in adults. … The patient was diagnosed as having alveolar rhabdomyosarcoma. … We conclude that rhabdomyosarcoma should be included in the differential diagnoses of CD56<SUP>+</SUP> …
- NAID 10023917300
Related Links
- 21 Jun 2011 ... Alveolar rhabdomyosarcoma (ARMS) typically affects older children or teenagers and occurs more often in large muscles of the trunk, arms, and legs. ARMS cells look like the normal muscle cells seen in a 10-week-old fetus. ...
Related Pictures
★リンクテーブル★
[★]
- 英
- alveolar rhabdomyosarcoma
- 関
- 胞巣状横紋筋肉腫
[★]
- 英
- alveolar rhabdomyosarcoma
- 関
- 胞巣型横紋筋肉腫
[★]
- 関
- alveoli、alveolus、pulmonary alveoli、pulmonary alveolus、tooth socket