Rhabdomyosarcoma, Spindle Cell/Sclerosing Variant: A Clinical and Histopathological Examination of this Rare Variant with Three New Cases from the Oral Cavity
Sign Up to like & getrecommendations! Published in 2017 at "Head and Neck Pathology"
DOI: 10.1007/s12105-017-0818-x
Abstract: Spindle cell/sclerosing rhabdomyosarcoma (S-ScRMS) was recently recognized in 2013 by the World Health Organization (WHO) as a stand-alone entity (Parham et al., WHO classification of tumours of soft tissue and bone, IARC Press, Lyon, 2013).… read more here.
Keywords: three new; spindle cell; rhabdomyosarcoma; new cases ... See more keywords
Challenges in the Diagnosis of Pediatric Spindle Cell/Sclerosing Rhabdomyosarcoma.
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DOI: 10.1016/j.path.2020.08.010
Abstract: Rhabdomyosarcoma (RMS) is the most common pediatric soft tissue sarcoma, representing approximately 40% of all pediatric soft tissue sarcomas. The spindle cell/sclerosing subtype of RMS (SSRMS) accounts for roughly 5% to 10% of all cases… read more here.
Keywords: challenges diagnosis; spindle cell; rhabdomyosarcoma; cell sclerosing ... See more keywords
Spindle Cell/Sclerosing Rhabdomyosarcoma With PAX8::PPARG Fusion
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DOI: 10.1177/10668969221095170
Abstract: The spindle cell/sclerosing subtype of rhabdomyosarcoma is classified based on genetic features into the three categories of MYOD1-mutated, gene fusion-driven, and a subset without a currently identified genetic driver event. The gene fusion-driven spindle cell/sclerosing… read more here.
Keywords: cell sclerosing; fusion; spindle cell; pax8 pparg ... See more keywords