Skip to search formSkip to main content
You are currently offline. Some features of the site may not work correctly.

Spindle Cell/Sclerosing Rhabdomyosarcoma

An uncommon variant of rhabdomyosarcoma with spindle cell or sclerosing morphology. It affects both children and adults and it is more common in… Expand
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
Objective: To study the clinicopathological features and immunophenotype of spindle cell/sclerosing rhabdomyosarcoma (SRMS) in… Expand
Review
2019
Review
2019
Rhabdomyosarcomas are malignancies associated with a rhabdomyoblastic phenotype which can be demonstrated morphologically or by… Expand
  • table 1
  • figure 3
  • table 2
2018
2018
Sclerosing and spindle cell rhabdomyosarcoma is a rare histologic subtype, designated in the latest WHO classification as a stand… Expand
  • table 1
  • figure 1
  • figure 2
  • figure 3
  • figure 4
2018
2018
Rhabdomyosarcomas of bone are extremely rare, with fewer than 10 reported cases. A very rare subtype of spindle cell/sclerosing… Expand
2018
2018
Ewing sarcoma (ES) is a round cell sarcoma that can be challenging to diagnose on cytologic material given its significant… Expand
2018
2018
The diagnosis of mesenchymal chondrosarcoma, a distinctive biphasic malignant neoplasm harboring the HEY1-NCOA2 gene fusion and… Expand
2018
2018
Recently, spindle cell/sclerosing rhabdomyosarcoma (SRMS/ScRMS) has been recognized as a stand-alone entity in the latest edition… Expand
2016
2016
Abstract Rhabdomyosarcoma is the most common malignancy of soft tissue in childhood and adolescence. It has been traditionally… Expand
  • figure 4
  • figure 1
  • figure 2
  • figure 3
2015
2015
Clinical characteristics and optimal treatment strategies for spindle cell/sclerosing rhabdomyosarcoma (ssRMS) have not been well… Expand
2014
2014
Recently, spindle cell/sclerosing rhabdomyosarcoma (RMS) has been recognized as another distinct variant of a RMS. We evaluated… Expand