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Spindle Cell Rhabdomyosarcoma

An uncommon variant of rhabdomyosarcoma characterized by the presence of whorls of spindle cells forming a storiform pattern. In children it usually… 
National Institutes of Health

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13 relations
Connective Tissue CellsConnective and Soft TissueEpithelial CellsEpithelium

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2018
Highly Cited
2018
MYOD1-mutant spindle cell and sclerosing rhabdomyosarcoma: an aggressive subtype irrespective of age. A reappraisal for molecular classification and risk stratification
Sclerosing and spindle cell rhabdomyosarcoma is a rare histologic subtype, designated in the latest WHO classification as a stand… 
2018
2018
Spindle cell rhabdomyosarcoma of bone with FUS–TFCP2 fusion: confirmation of a very recently described rhabdomyosarcoma subtype
Rhabdomyosarcomas of bone are extremely rare, with fewer than 10 reported cases. A very rare subtype of spindle cell/sclerosing… 
Highly Cited
2016
Highly Cited
2016
MYOD1 (L122R) mutations are associated with spindle cell and sclerosing rhabdomyosarcomas with aggressive clinical outcomes
Recurrent mutations in the myogenic transcription factor MYOD1 and PIK3CA were initially described in a subset of embryonal… 
Highly Cited
2015
Highly Cited
2015
A Molecular Study of Pediatric Spindle and Sclerosing Rhabdomyosarcoma: Identification of Novel and Recurrent VGLL2-related Fusions in Infantile Cases
Sclerosing rhabdomyosarcoma (ScRMS) and spindle cell rhabdomyosarcoma (SRMS) have been recently reclassified as a stand-alone… 
Highly Cited
2014
Highly Cited
2014
Recurrent MYOD1 mutations in pediatric and adult sclerosing and spindle cell rhabdomyosarcomas: Evidence for a common pathogenesis
Sclerosing and spindle cell rhabdomyosarcoma (RMS) are rare types of RMS recently reclassified as a stand‐alone pathologic entity… 
Highly Cited
2014
Highly Cited
2014
Transactivating mutation of the MYOD1 gene is a frequent event in adult spindle cell rhabdomyosarcoma
Rhabdomyosarcoma (RMS) is the most common soft‐tissue sarcoma in children and adolescents, being characterized by expression of… 
Highly Cited
2013
Highly Cited
2013
Recurrent NCOA2 gene rearrangements in congenital/infantile spindle cell rhabdomyosarcoma
Spindle cell rhabdomyosarcoma (RMS) is a rare form of RMS with different clinical characteristics between children and adult… 
Review
2006
Review
2006
Rhabdomyosarcomas in adults and children: an update.
CONTEXT Rhabdomyosarcomas comprise a relatively common diagnostic entity among childhood cancers and a relatively rare one among… 
Highly Cited
2005
Highly Cited
2005
Spindle Cell Rhabdomyosarcoma in Adults
The spindle cell variant of rhabdomyosarcoma (RMS) is uncommon and is most often encountered in the paratesticular region of… 
Highly Cited
1992
Highly Cited
1992
Spindle Cell Rhabdomyosarcoma: A Prognostically Favorable Variant of Rhabdomyosarcoma
Twenty-one cases of embryonal rhabdomyosarcoma, composed mainly of elongated spindle cells arranged in a fasciculated or… 
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