Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 210,023,917 papers from all fields of science
Search
Sign In
Create Free Account
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…
Expand
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
13 relations
Connective Tissue Cells
Connective and Soft Tissue
Epithelial Cells
Epithelium
Expand
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
Narasimhan P. Agaram
,
M. LaQuaglia
,
+5 authors
C. Antonescu
Modern Pathology
2018
Corpus ID: 52153480
Sclerosing and spindle cell rhabdomyosarcoma is a rare histologic subtype, designated in the latest WHO classification as a stand…
Expand
2018
2018
Spindle cell rhabdomyosarcoma of bone with FUS–TFCP2 fusion: confirmation of a very recently described rhabdomyosarcoma subtype
N. Dashti
,
Rebecca N. Wehrs
,
+8 authors
A. Folpe
Histopathology
2018
Corpus ID: 46887889
Rhabdomyosarcomas of bone are extremely rare, with fewer than 10 reported cases. A very rare subtype of spindle cell/sclerosing…
Expand
Highly Cited
2016
Highly Cited
2016
MYOD1 (L122R) mutations are associated with spindle cell and sclerosing rhabdomyosarcomas with aggressive clinical outcomes
B. Rekhi
,
P. Upadhyay
,
Manoj P. Ramteke
,
A. Dutt
Modern Pathology
2016
Corpus ID: 12289621
Recurrent mutations in the myogenic transcription factor MYOD1 and PIK3CA were initially described in a subset of embryonal…
Expand
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
R. Alaggio
,
Lei Zhang
,
+8 authors
C. Antonescu
American Journal of Surgical Pathology
2015
Corpus ID: 6411331
Sclerosing rhabdomyosarcoma (ScRMS) and spindle cell rhabdomyosarcoma (SRMS) have been recently reclassified as a stand-alone…
Expand
Highly Cited
2014
Highly Cited
2014
Recurrent MYOD1 mutations in pediatric and adult sclerosing and spindle cell rhabdomyosarcomas: Evidence for a common pathogenesis
Narasimhan P. Agaram
,
Chun‐Liang Chen
,
Lei Zhang
,
M. LaQuaglia
,
L. Wexler
,
C. Antonescu
Genes, Chromosomes and Cancer
2014
Corpus ID: 29213879
Sclerosing and spindle cell rhabdomyosarcoma (RMS) are rare types of RMS recently reclassified as a stand‐alone pathologic entity…
Expand
Highly Cited
2014
Highly Cited
2014
Transactivating mutation of the MYOD1 gene is a frequent event in adult spindle cell rhabdomyosarcoma
K. Szuhai
,
D. de Jong
,
Wai Y Leung
,
C. Fletcher
,
P. Hogendoorn
Journal of Pathology
2014
Corpus ID: 25713132
Rhabdomyosarcoma (RMS) is the most common soft‐tissue sarcoma in children and adolescents, being characterized by expression of…
Expand
Highly Cited
2013
Highly Cited
2013
Recurrent NCOA2 gene rearrangements in congenital/infantile spindle cell rhabdomyosarcoma
J. Mosquera
,
A. Sboner
,
+9 authors
C. Antonescu
Genes, Chromosomes and Cancer
2013
Corpus ID: 26618281
Spindle cell rhabdomyosarcoma (RMS) is a rare form of RMS with different clinical characteristics between children and adult…
Expand
Review
2006
Review
2006
Rhabdomyosarcomas in adults and children: an update.
D. Parham
,
D. A. Ellison
Archives of Pathology & Laboratory Medicine
2006
Corpus ID: 22158911
CONTEXT Rhabdomyosarcomas comprise a relatively common diagnostic entity among childhood cancers and a relatively rare one among…
Expand
Highly Cited
2005
Highly Cited
2005
Spindle Cell Rhabdomyosarcoma in Adults
A. Nascimento
,
C. Fletcher
American Journal of Surgical Pathology
2005
Corpus ID: 10384930
The spindle cell variant of rhabdomyosarcoma (RMS) is uncommon and is most often encountered in the paratesticular region of…
Expand
Highly Cited
1992
Highly Cited
1992
Spindle Cell Rhabdomyosarcoma: A Prognostically Favorable Variant of Rhabdomyosarcoma
A. Cavazzana
,
D. Schmidt
,
+6 authors
G. Salviati
American Journal of Surgical Pathology
1992
Corpus ID: 40989010
Twenty-one cases of embryonal rhabdomyosarcoma, composed mainly of elongated spindle cells arranged in a fasciculated or…
Expand
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE