"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
|
| MeSH Number(s) |
C04.557.435.710
|
| Concept/Terms |
Rhabdoid Tumor- Rhabdoid Tumor
- Rhabdoid Tumors
- Tumor, Rhabdoid
- Tumors, Rhabdoid
|
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.
View timeline visualization
| Year | Major Topic | Minor Topic | Total |
|---|
| 1995 | 3 | 0 | 3 |
| 1996 | 2 | 0 | 2 |
| 1998 | 2 | 0 | 2 |
| 1999 | 2 | 1 | 3 |
| 2000 | 2 | 0 | 2 |
| 2001 | 1 | 0 | 1 |
| 2002 | 6 | 0 | 6 |
| 2003 | 2 | 0 | 2 |
| 2004 | 5 | 2 | 7 |
| 2005 | 4 | 2 | 6 |
| 2006 | 5 | 1 | 6 |
| 2007 | 7 | 0 | 7 |
| 2008 | 4 | 3 | 7 |
| 2009 | 9 | 1 | 10 |
| 2010 | 6 | 1 | 7 |
| 2011 | 5 | 2 | 7 |
| 2012 | 3 | 4 | 7 |
| 2013 | 2 | 0 | 2 |
| 2014 | 6 | 3 | 9 |
| 2015 | 7 | 1 | 8 |
| 2016 | 6 | 2 | 8 |
| 2017 | 4 | 1 | 5 |
| 2018 | 2 | 0 | 2 |
| 2019 | 2 | 0 | 2 |
| 2020 | 9 | 0 | 9 |
| 2021 | 3 | 1 | 4 |
| 2022 | 5 | 0 | 5 |
| 2023 | 7 | 0 | 7 |
| 2024 | 3 | 0 | 3 |
| 2025 | 1 | 0 | 1 |
Below are the most recent publications written about "Rhabdoid Tumor" by people in Profiles.
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Extra-renal non-cerebral malignant rhabdoid tumor in children: does maintenance chemotherapy play a role in survival? Medicina (B Aires). 2025; 85(1):101-111.
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Rhabdoid Tumor of the Kidney and Soft Tissues: Results from National Wilms Tumor Study-5 and Children's Oncology Group Study AREN0321. Pediatr Blood Cancer. 2025 Mar; 72(3):e31490.
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Autologous stem cell transplantation in adults with atypical teratoid rhabdoid tumor: a case report and review. CNS Oncol. 2024 Dec 31; 13(1):2375960.
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Sarcomatoid and Rhabdoid Renal Cell Carcinoma: Clinical, Pathologic, and Molecular Genetic Features. Am J Surg Pathol. 2024 Jul 01; 48(7):e65-e88.
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Targeting of RRM2 suppresses DNA damage response and activates apoptosis in atypical teratoid rhabdoid tumor. J Exp Clin Cancer Res. 2023 Dec 20; 42(1):346.
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Tazemetostat for tumors harboring SMARCB1/SMARCA4 or EZH2 alterations: results from NCI-COG pediatric MATCH APEC1621C. J Natl Cancer Inst. 2023 11 08; 115(11):1355-1363.
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Rhabdoid tumors in patients conceived following ART: is there an association? Hum Reprod. 2023 10 03; 38(10):2028-2038.
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Children's Oncology Group's 2023 blueprint for research: Renal tumors. Pediatr Blood Cancer. 2023 09; 70 Suppl 6:e30586.
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Optical genome mapping identifies a novel pediatric embryonal tumor with a ZNF532::NUTM1 fusion. J Pathol. 2023 07; 260(3):329-338.
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Radiotherapy for Atypical Teratoid/Rhabdoid Tumor (ATRT) on the Pediatric Proton/Photon Consortium Registry (PPCR). J Neurooncol. 2023 Apr; 162(2):353-362.