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

Atypical teratoid rhabdoid tumor in the cavernous sinus of a toddler presenting with oculomotor nerve palsy.
 

Author(s): Nami Inoue, Hiroyoshi Watanabe, Kazumi Okamura, Mika Sakaki, Teruyoshi Kageji, Shinji Nagahiro, Shoji Kagami

Journal: Childs Nerv Syst. 2014 Aug;30(8):1463-6.

 

Atypical teratoid rhabdoid tumor (ATRT) is a rare, highly malignant, and aggressive tumor of infancy. Although the prognosis of ATRT has been extremely poor, recently, the first prospective study for ATRT demonstrated improvement of prognosis. On the other hands, oculomotor nerve ...

Last Updated: 18 Jul 2014

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Frequent overexpression of HMGA2 in human atypical teratoid/rhabdoid tumor and its correlation with let-7a3/let-7b miRNA.
 

Author(s): Keqiang Zhang, Hanlin Gao, Xiwei Wu, Jinhui Wang, Wendi Zhou, Guihua Sun, Jinghan Wang, Yafan Wang, Bing Mu, Charles Kim, Peiguo Chu, Donald M Ho, David K Ann, Tai-Tong Wong, Yun Yen

Journal: Clin. Cancer Res.. 2014 Mar;20(5):1179-89.

 

Atypical teratoid/rhabdoid tumors (AT/RT) are highly aggressive pediatric malignancies characterized by biallelic inactivation of the SMARCB1 tumor suppressor gene. We searched for novel genomic aberrations by investigating the copy number and expression alterations of let-7a3/let-7b ...

Last Updated: 4 Mar 2014

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Atypical teratoid rhabdoid tumor: improved long-term survival with an intensive multimodal therapy and delayed radiotherapy. The Medical University of Vienna Experience 1992-2012.
 

Author(s): Irene Slavc, Monika Chocholous, Ulrike Leiss, Christine Haberler, Andreas Peyrl, Amedeo A Azizi, Karin Dieckmann, Adelheid Woehrer, Christina Peters, Georg Widhalm, Christian Dorfer, Thomas Czech

Journal: Cancer Med. 2014 Feb;3(1):91-100.

 

Atypical teratoid rhabdoid tumors (ATRTs) are recently defined highly aggressive embryonal central nervous system tumors with a poor prognosis and no definitive guidelines for treatment. We report on the importance of an initial correct diagnosis and disease-specific therapy on outcome ...

Last Updated: 18 Mar 2014

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

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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Atypical teratoid rhabdoid tumor in adulthood.
 

Author(s): Cyrine Souki, Majdi Abdel-Rhaman, Adnan Qasem, Maysa Al-Hussaini

Journal: Clin. Neuropathol.. ;33(3):245-50.

 

Last Updated: 30 Apr 2014

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Cytomorphology and immunohistochemistry of extrarenal rhabdoid tumor: a case report with review of literature.
 

Author(s): Manjula Jain, Aparna Harbhajanka, S Roy Choudhary

Journal: Indian J Pathol Microbiol. ;54(4):819-21.

 

Extrarenal rhabdoid tumor (ERRT) is a rare, aggressive tumor with extremely poor prognosis. We report a case of ERRT with intraspinal extension in a 1.5-year-old child diagnosed by fine needle aspiration cytology (FNAC) and immunohistochemistry. The child presented with a right lumbar ...

Last Updated: 11 Jan 2012

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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: 10 Jul 2015

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A Study of CD45RA+ Depleted Haploidentical Stem Cell Transplantation in Children With Relapsed or Refractory Solid Tumors and Lymphomas
 

Status: Recruiting

Condition Summary: Ewing Sarcoma; Gastrointestinal Tumor; Germ Cell Tumor; Hepatic Tumor; Lymphoma; Wilms Tumor; Rhabdoid Tumor; Clear Cell Carcinoma; Renal Cell Carcinoma; Melanoma; Neuroblastoma; Rhabdomyosarcoma; Non-rhabdomyosarcoma

 

Last Updated: 28 May 2015

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Simvastatin With Topotecan and Cyclophosphamide in Relapsed and/or Refractory Pediatric Solid and CNS Tumors
 

Status: Recruiting

Condition Summary: Retinoblastoma; Clear Cell Sarcoma; Renal Cell Carcinoma; Rhabdoid Tumor; Wilms Tumor; Hepatoblastoma; Neuroblastoma; Germ Cell Tumors; Ewings Sarcoma; Non-rhabdomyosarcoma Soft Tissue Sarcoma; Osteosarcoma; Rhabdomyosarcoma

 

Last Updated: 11 Mar 2015

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