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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… Expand
National Institutes of Health

Related topics

Related topics

12 relations
Connective Tissue CellsConnective and Soft TissueEpithelial CellsEpithelium
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Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2014
Highly Cited
2014
Soft tissue and visceral sarcomas: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up.
Extraskeletal Ewing sarcoma is covered by other ESMO Guidelines: in general, the same principles for these tumours in children… Expand
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Highly Cited
2006
Highly Cited
2006
Cooperation of oncogenic K-ras and p53 deficiency in pleomorphic rhabdomyosarcoma development in adult mice
Human rhabdomyosarcomas (RMSs) frequently demonstrate genetic alterations in ras and p53. To investigate their possible… Expand
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Highly Cited
1995
Highly Cited
1995
Multiplex RT-PCR assay for the differential diagnosis of alveolar rhabdomyosarcoma and Ewing's sarcoma.
Cytogenetic analysis has defined specific translocations associated with two of the most common small round cell tumors of… Expand
1994
1994
Carcinosarcoma (malignant mixed tumor) of the parotid: Report of a case with a pure rhabdomyosarcoma component
Background. Carcinosarcoma or true malignant mixed tumor of the parotid gland is extremely rare, accounting for <1% of all… Expand
Review
1994
Review
1994
The diagnosis and classification of childhood rhabdomyosarcoma.
  • M. Tsokos
  • Seminars in diagnostic pathology
  • 1994
    • Corpus ID: 13487788
Although the typical subtypes of embryonal, botryoid, alveolar, and pleomorphic rhabdomyosarcoma are easily recognized by simple… Expand
Highly Cited
1993
Highly Cited
1993
Pleomorphic Rhabdomyosarcoma in Adulthood: Analysis of 11 Cases with Definition of Diagnostic Criteria
Currently, pleomorphic rhabdomyosarcoma (RMS) in adults is considered to be extremely rare or nonexistent. The authors have… Expand
1987
1987
Pleomorphic rhabdomyosarcoma in adults: immunohistochemistry as a tool for its diagnosis.
Pleomorphic rhabdomyosarcoma in adults over 30 years of age was a diagnosis frequently made in the 1960s and 1970s. Since the… Expand
Highly Cited
1979
Highly Cited
1979
Malignant soft tissue tumors (malignant fibrous histiocytoma, pleomorphic liposarcoma, and pleomorphic rhabdomyosarcoma): an electron microscopic study.
A comparative ultrastructural analysis of malignant soft tissue tumors (malignant fibrous histiocytoma, pleomorphic liposarcoma… Expand
Highly Cited
1977
Highly Cited
1977
Pleomorphic carcinoma of the pancreas. An analysis of 15 cases
Pleomorphic carcinoma of the pancreas is a well defined histopathological entity characterized by non‐cohesive, sarcoma‐like… Expand
Highly Cited
1973
Highly Cited
1973
Peripheral nerve tumors with rhabdomyosarcomatous differentiation (malignant “triton” tumors)
Three peripheral nerve sheath tumors are reported which showed an intermingling of schwannian elements and rhabdomyosarcoma, a… Expand
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