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.

There are currently no organizations listed in Disease InfoSearch that support this condition. Create a listing.

 

 

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 108 free, full-text research articles on human participants. First 3 results:

Phosphoproteomic analysis reveals Smarcb1 dependent EGFR signaling in Malignant Rhabdoid tumor cells.
 

Author(s): Jonatan Darr, Agnes Klochendler, Sara Isaac, Tamar Geiger, Tami Geiger, Amir Eden

Journal:

 

The SWI/SNF ATP dependent chromatin remodeling complex is a multi-subunit complex, conserved in eukaryotic evolution that facilitates nucleosomal re-positioning relative to the DNA sequence. In recent years the SWI/SNF complex has emerged to play a role in cancer development as various ...

Last Updated: 15 Sep 2015

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Atypical teratoid/rhabdoid tumor (ATRT) arising from the 3rd cranial nerve in infants: a clinical-radiological entity?
 

Author(s): Christopher C Oh, Brent A Orr, Bruno Bernardi, Maria Luisa Garré, Andrea Rossi, Lorenzo Figà-Talamanca, Giles W Robinson, Zoltán Patay

Journal: J. Neurooncol.. 2015 Sep;124(2):175-83.

 

Atypical teratoid/rhabdoid tumor (ATRT) is a rare embryonal tumor of the central nervous system with preponderance in very young children, the majority of whom are younger than 3 years of age at diagnosis. Historically, outcomes of this aggressive disease, even with extensive multimodal ...

Last Updated: 25 Sep 2015

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[About a rare case of atypical rhabdoid teratoid tumor of the central nervous system in a pregnant woman].
 

Author(s): Mohammed Afif, Jihane Khalil, Fadila Kouhen, Abdellah Aissa, Youssef Omour, Mustapha Elkabous, Hanan Elkacemi, Tayeb Kebdani, Noureddine Benjaafar

Journal:

 

Last Updated: 21 May 2015

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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 11 free, full-text review articles on human participants. First 3 results:

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: 27 Apr 2015

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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: 30 Jan 2015

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Primary atypical teratoid/rhabdoid tumor of central nervous system in children: a clinicopathological analysis and review of literature in China.
 

Author(s): Min Yang, Xi Chen, Ning Wang, Kun Zhu, Ying-Zi Hu, Yun Zhao, Yan Shu, Man-Li Zhao, Wei-Zhong Gu, Hong-Feng Tang

Journal:

 

Atypical teratoid/rhabdoid tumor (AT/RT) is a very rare and highly malignant embryonal tumor in the central nervous system (CNS). Five patients (4 girls and 1 boy) with AT/RT were treated in our hospital. The clinical histories, symptoms, neuroimaging aspects, therapies, histological ...

Last Updated: 26 Jun 2014

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Symptoms, Diagnosis, and Treatment

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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: 4 May 2016

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A Phase II, Multicenter Study of the EZH2 Inhibitor Tazemetostat in Adult Subjects With INI1-Negative Tumors or Relapsed/Refractory Synovial Sarcoma
 

Status: Recruiting

Condition Summary: Malignant Rhabdoid Tumors (MRT); Rhabdoid Tumors of the Kidney (RTK); Atypical Teratoid Rhabdoid Tumors (ATRT); Selected Tumors With Rhabdoid Features; Synovial Sarcoma; INI1-negative Tumors; Malignant Rhabdoid Tumor of Ovary; Renal Medullary Carcinoma; Epithelioid Sarcoma

 

Last Updated: 20 Sep 2016

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Tazemetostat Rollover Study (TRuST): An Open-Label Rollover Study
 

Status: Recruiting

Condition Summary: Diffuse Large B-cell Lymphoma; Follicular Lymphoma; Malignant Rhabdoid Tumors (MRT); Rhabdoid Tumors of the Kidney (RTK); Atypical Teratoid Rhabdoid Tumors (ATRT); Synovial Sarcoma; Epitheliod Sarcoma; Mesothelioma; Advanced Solid Tumors

 

Last Updated: 13 Sep 2016

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