Rhabdomyosarcoma alveolar

Common Name(s)

Rhabdomyosarcoma alveolar

Description for this condition is not yet available.
 

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Advocacy and Support Organizations

 

Condition Specific Organizations

Following organizations serve the condition "Rhabdomyosarcoma alveolar" 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 "Rhabdomyosarcoma alveolar" returned 121 free, full-text research articles on human participants. First 3 results:

Primary alveolar rhabdomyosarcoma of the bone: two cases and review of the literature.
 

Author(s): Petra Balogh, Rita Bánusz, Monika Csóka, Zsófia Váradi, Edit Varga, Zoltán Sápi

Journal:

 

Rhabdomyosarcoma (RMS) is a malignant tumor of mesenchymal origin and comprises the largest category of soft-tissue sarcomas both in children and adolescents. From a pediatric oncology point of view, RMS has traditionally been classified into alveolar (ARMS) and embryonal (ERMS) subtypes. ...

Last Updated: 19 Oct 2016

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Histology, Fusion Status, and Outcome in Alveolar Rhabdomyosarcoma With Low-Risk Clinical Features: A Report From the Children's Oncology Group.
 

Author(s): Michael A Arnold, James R Anderson, Julie M Gastier-Foster, Frederic G Barr, Stephen X Skapek, Douglas S Hawkins, R Beverly Raney, David M Parham, Lisa A Teot, Erin R Rudzinski, David O Walterhouse

Journal: Pediatr Blood Cancer. 2016 Apr;63(4):634-9.

 

Distinguishing alveolar rhabdomyosarcoma (ARMS) from embryonal rhabdomyosarcoma (ERMS) is of prognostic and therapeutic importance. Criteria for classifying these entities evolved significantly from 1995 to 2013. ARMS is associated with inferior outcome; therefore, patients with alveolar ...

Last Updated: 16 Feb 2016

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Crizotinib-induced antitumour activity in human alveolar rhabdomyosarcoma cells is not solely dependent on ALK and MET inhibition.
 

Author(s): Francesca Megiorni, Heather P McDowell, Simona Camero, Olga Mannarino, Simona Ceccarelli, Milena Paiano, Paul D Losty, Barry Pizer, Rajeev Shukla, Antonio Pizzuti, Anna Clerico, Carlo Dominici

Journal:

 

Rhabdomyosarcoma (RMS) is the most commonly diagnosed malignant soft tissue tumour in children and adolescents. Aberrant expression of Anaplastic Lymphoma Kinase (ALK) and MET gene has been implicated in the malignant progression of RMS, especially in the alveolar subtype. This observation ...

Last Updated: 8 Oct 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 "Rhabdomyosarcoma alveolar" returned 6 free, full-text review articles on human participants. First 3 results:

Alveolar rhabdomyosarcoma of nasopharynx and paranasal sinuses with metastasis to breast in a middle-aged woman: a case report and literature review.
 

Author(s): Hongmei Liu, Wei Zhao, Meijuan Huang, Xiaojuan Zhou, Youling Gong, You Lu

Journal:

 

Alveolar rhabdomyosarcoma (ARMS) is a common soft tissue tumor in children which can rarely metastasize to the breast in adults. Here we report the rare case of a 42-year-old Asian woman, who was diagnosed with ARMS of the nasopharynx and paranasal sinuses, and got a complete remission ...

Last Updated: 29 Jan 2016

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Primary alveolar rhabdomyosarcoma of fallopian tube masquerading as a unilateral adnexal mass: A case report and literature review.
 

Author(s): Nisreen Abu Shahin, Amin Alqaisy, Wenxin Zheng

Journal: Indian J Pathol Microbiol. ;58(4):521-3.

 

Rhabdomyosarcoma (RMS) is a high-grade sarcoma that predominantly affects children, and rarely, the adult population. RMS demonstrates three major histologic variants: Embryonal, alveolar, and pleomorphic. A limited number of documented pure RMS cases of the gynecologic organs in ...

Last Updated: 9 Nov 2015

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Alveolar rhabdomyosarcoma with multiple distal metastases. A case report and review of literature.
 

Author(s): Debojyoti Sarkar, Sayantan Ray, Manjari Saha, Prantar Chakrabarti, Prantari Chakrabarti

Journal:

 

An 18-year-old boy, presented with a history of right hip pain with movement restriction and proptosis of right eye. There was severe anaemia, febrile neutropaenia and bleeding manifestations. CT scan of right orbit documented a retro orbital mass. MRI revealed a mass on right side ...

Last Updated: 5 Sep 2012

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Clinical Trial Information This information is provided by ClinicalTrials.gov

Last Updated: 22 Jun 2017

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A Two-Part Study of TB-403 in Pediatric Subjects With Relapsed or Refractory Medulloblastoma
 

Status: Recruiting

Condition Summary: Relapsed or Refractory Medulloblastoma (MB) (Part A: Also Include Neuroblastoma (NB), Ewing Sarcoma (ES) and Alveolar Rhabdomyosarcoma (ARMS))

 

Last Updated: 21 Feb 2017

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CREATE: Cross-tumoral Phase 2 With Crizotinib
 

Status: Recruiting

Condition Summary: Locally Advanced and/or Metastatic Anaplastic Large Cell Lymphoma; Locally Advanced and/or Metastatic Inflammatory Myofibroblastic Tumor; Locally Advanced and/or Metastatic Papillary Renal Cell Carcinoma Type 1; Locally Advanced and/or Metastatic Alveolar Soft Part Sarcoma; Locally Advanced and/or Metastatic Clear Cell Sarcoma; Locally Advanced and/or Metastatic Alveolar Rhabdomyosarcoma

 

Last Updated: 6 Jul 2016

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