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pleomorphic rhabdomyosarcoma

Known as: rhabdomyosarcoma pleomorphic 
An aggressive malignant mesenchymal neoplasm with skeletal muscle differentiation, occurring in adults and rarely in children. The tumor is… 
National Institutes of Health

Papers overview

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Review
2019
Review
2019
Rhabdomyosarcomas are malignancies associated with a rhabdomyoblastic phenotype which can be demonstrated morphologically or by… 
Highly Cited
2014
Highly Cited
2014
Extraskeletal Ewing sarcoma is covered by other ESMO Guidelines: in general, the same principles for these tumours in children… 
Review
2001
Review
2001
Pleomorphic rhabdomyosarcoma (PRMS) is a rare and controversial tumor of skeletal muscle phenotype. Diagnostic criteria for PRMS… 
Highly Cited
1995
Highly Cited
1995
Cytogenetic analysis has defined specific translocations associated with two of the most common small round cell tumors of… 
1994
1994
Background. Carcinosarcoma or true malignant mixed tumor of the parotid gland is extremely rare, accounting for <1% of all… 
Highly Cited
1993
Highly Cited
1993
Currently, pleomorphic rhabdomyosarcoma (RMS) in adults is considered to be extremely rare or nonexistent. The authors have… 
Review
1986
Review
1986
Highly Cited
1977
Highly Cited
1977
Pleomorphic carcinoma of the pancreas is a well defined histopathological entity characterized by non‐cohesive, sarcoma‐like… 
Highly Cited
1973
Highly Cited
1973
Three peripheral nerve sheath tumors are reported which showed an intermingling of schwannian elements and rhabdomyosarcoma, a…