Rhabdoid tumor

Common Name(s)

Rhabdoid tumor

Description for this condition is not yet available.
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Rhabdoid tumor" for support, advocacy or research.

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General Support Organizations

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Scientific Literature

Articles from the PubMed Database

Research articles describe the outcome of a single study. They are the published results of original research.
The terms "Rhabdoid tumor" returned 111 free, full-text research articles on human participants. First 3 results:

Timing of Smarcb1 and Nf2 inactivation determines schwannoma versus rhabdoid tumor development.
 

Author(s): Jeremie Vitte, Fuying Gao, Giovanni Coppola, Alexander R Judkins, Marco Giovannini

Journal:

 

Germline mutations of the SMARCB1 gene predispose to two distinct tumor syndromes: rhabdoid tumor predisposition syndrome, with malignant pediatric tumors mostly developing in brain and kidney, and familial schwannomatosis, with adulthood benign tumors involving cranial and peripheral ...

Last Updated: 31 Dec 1969

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Deep intronic hotspot variant explaining rhabdoid tumor predisposition syndrome in two patients with atypical teratoid and rhabdoid tumor.
 

Author(s): Arnault Tauziède-Espariat, Julien Masliah-Planchon, Laurence Brugières, Stéphanie Puget, Christelle Dufour, Pascale Schneider, Annie Laquerrière, Thierry Frebourg, Damien Bodet, Emmanuèle Lechapt-Zalcman, Gaëlle Pierron, Olivier Delattre, Pascale Varlet, Franck Bourdeaut

Journal: Eur. J. Hum. Genet.. 2017 10;25(10):1170-1172.

 

About one third of patients with rhabdoid tumors (RT) harbor a heterozygous germline variant in SMARCB1. Molecular diagnosis therefore keeps a crucial place in the diagnosis of RT, and genetic counseling should be systematically recommended. However, immunohistochemistry has progressively ...

Last Updated: 31 Dec 1969

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Insulin-like growth factor 2 axis supports the serum-independent growth of malignant rhabdoid tumor and is activated by microenvironment stress.
 

Author(s): Ting Li, Jin Wang, Pengfei Liu, Jiadong Chi, Han Yan, Lei Lei, Zexing Li, Bing Yang, Xi Wang

Journal: Oncotarget. 2017 Jul;8(29):47269-47283.

 

Malignant rhabdoid tumors (MRTs) are rare, lethal, pediatric tumors predominantly found in the kidney, brain and soft tissues. MRTs are driven by loss of tumor suppressor SNF5/INI1/SMARCB1/BAF47. The prognosis of MRT is poor using currently available treatments, so new treatment targets ...

Last Updated: 31 Dec 1969

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Reviews from the PubMed Database

Review articles summarize what is currently known about a disease. They discuss research previously published by others.
The terms "Rhabdoid tumor" returned 12 free, full-text review articles on human participants. First 3 results:

Malignant rhabdoid tumor of the vulva: A case report and review of the literature.
 

Author(s): Mehmet Dolanbay, Mehmet Serdar Kutuk, Semih Uludag, Mensure Tonguc, Bulent Ozcelik, Ibrahim Serdar Serin, Sinan Nazlım, Figen Ozturk

Journal: Taiwan J Obstet Gynecol. 2016 Feb;55(1):128-30.

 

Last Updated: 31 Dec 1969

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Atypical teratoid/rhabdoid tumor of the brain in an adult with 22q deletion but no absence of INI1 protein: a case report and review of the literature.
 

Author(s): S Jin, C Sun, S Yu, Q Wang, T An, Y Wen

Journal: Folia Neuropathol. 2015 ;53(1):80-5.

 

We report a case of atypical teratoid/rhabdoid tumor (AT/RT) of the central nervous system (CNS) in an adult and its immunological phenotype and chromosomal DNA imbalance characteristics, as detected by comparative genomic hybridization (CGH). The immunohistochemical characteristics ...

Last Updated: 31 Dec 1969

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Atypical teratoid/rhabdoid tumor (AT/RT) arising from the acoustic nerve in a young adult: a case report and a review of literature.
 

Author(s): Xingfu Wang, Xueyong Liu, Zhixiong Lin, Yupeng Chen, Pengcheng Wang, Sheng Zhang

Journal: Medicine (Baltimore). 2015 Jan;94(4):e439.

 

Atypical teratoid/rhabdoid tumors (AT/RTs) are rare, highly malignant central nervous system tumors that predominantly occur in young children. A 22-year-old woman presented with a 4-year history of relapsing tinnitus and gradual hearing loss. Neuroimaging revealed an enhanced intrinsic ...

Last Updated: 31 Dec 1969

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Clinical Trial Information This information is provided by ClinicalTrials.gov

Phase 2 Study of Alisertib Therapy for Rhabdoid Tumors
 

Status: Recruiting

Condition Summary: Malignant Rhabdoid Tumor; Atypical Teratoid Rhabdoid Tumor

 

Last Updated: 7 Mar 2018

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Modified Measles Virus (MV-NIS) for Children and Young Adults With Recurrent Medulloblastoma or Recurrent ATRT
 

Status: Recruiting

Condition Summary: Medulloblastoma, Childhood, Recurrent; Atypical Teratoid/Rhabdoid Tumor; Medulloblastoma Recurrent

 

Last Updated: 16 Feb 2018

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Study of Stored Tumor Samples in Young Patients With Brain Tumors
 

Status: Recruiting

Condition Summary: Brain and Central Nervous System Tumors

 

Last Updated: 8 Sep 2017

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