Rhabdoid Tumor [rhabdoidní nádor]
- Terms
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rabdoidní nádor
A rare but highly lethal childhood tumor found almost exclusively in infants. Histopathologically, it resembles RHABDOMYOSARCOMA but the tumor cells are not of myogenic origin. Although it arises primarily in the kidney, it may be found in other parts of the body. The rhabdoid cytomorphology is believed to be the expression of a very primitive malignant cell. (From Holland et al., Cancer Medicine, 3d ed, p2210)
- DUI
- D018335 MeSH Browser
- CUI
- M0027572
- History note
- 94
- Public note
- 94
Allowable subheadings
- BL
- blood
- BS
- blood supply
- CF
- cerebrospinal fluid
- CI
- chemically induced
- CH
- chemistry 1
- CL
- classification
- CO
- complications
- CN
- congenital
- DI
- diagnosis 11
- DG
- diagnostic imaging
- DH
- diet therapy
- DT
- drug therapy 3
- EC
- economics
- EM
- embryology
- EN
- enzymology
- EP
- epidemiology
- EH
- ethnology
- ET
- etiology
- GE
- genetics 11
- HI
- history
- IM
- immunology
- ME
- metabolism 5
- MI
- microbiology
- MO
- mortality 2
- NU
- nursing
- PS
- parasitology
- PA
- pathology 13
- PP
- physiopathology
- PC
- prevention & control
- PX
- psychology
- RT
- radiotherapy
- RH
- rehabilitation
- SC
- secondary
- SU
- surgery 1
- TH
- therapy 8
- UL
- ultrastructure
- UR
- urine
- VE
- veterinary
- VI
- virology
Rhabdoid Tumor Predisposition Syndrome 1 Disease MeSH Browser
Rhabdoid Tumor Predisposition Syndrome 2 Disease MeSH Browser
Teratoid Tumor, Atypical Disease MeSH Browser
Typical Teratoid Rhabdoid Tumor Disease MeSH Browser