 Rhabdoid Tumor
"Rhabdoid Tumor" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
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)
| Descriptor ID |
D018335
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| MeSH Number(s) |
C04.557.435.710
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| Concept/Terms |
Rhabdoid Tumor- Rhabdoid Tumor
- Rhabdoid Tumors
- Tumor, Rhabdoid
- Tumors, Rhabdoid
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Below are MeSH descriptors whose meaning is more general than "Rhabdoid Tumor".
Below are MeSH descriptors whose meaning is more specific than "Rhabdoid Tumor".
This graph shows the total number of publications written about "Rhabdoid Tumor" by people in this website by year, and whether "Rhabdoid Tumor" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2016 | 1 | 0 | 1 |
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Below are the most recent publications written about "Rhabdoid Tumor" by people in Profiles.
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Farber BA, Shukla N, Lim II, Murphy JM, La Quaglia MP. Prognostic factors and survival in non-central nervous system rhabdoid tumors. J Pediatr Surg. 2017 Mar; 52(3):373-376.
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Ng JM, Martinez D, Marsh ED, Zhang Z, Rappaport E, Santi M, Curran T. Generation of a mouse model of atypical teratoid/rhabdoid tumor of the central nervous system through combined deletion of Snf5 and p53. Cancer Res. 2015 Nov 01; 75(21):4629-39.
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