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1.
Neurol Perspect ; 2(1): 47-48, 2022.
Article in English | MEDLINE | ID: mdl-38620868
2.
Genet Mol Res ; 8(4): 1211-7, 2009 Oct 06.
Article in English | MEDLINE | ID: mdl-19866439

ABSTRACT

Epithelioid sarcoma is a rare, aggressive soft tissue tumor of unknown histogenesis showing predominantly epithelioid cytomorphology. We conducted a conventional and molecular cytogenetic study of a 27-year-old male with epithelioid sarcoma with angiomatoid features. Cytogenetic analysis of epithelioid sarcoma metaphase spreads by GTG-banding revealed a diploid chromosome complement with structural and numerical aberrations. Comparative genomic hybridization analysis demonstrated the amplification of 3p24-pter, 4p15.2-p16 and 18q23, while chromosome losses involved 3p13-p14, 3q24-q26.1, 9q21, and 11q21. Fluorescence in situ hybridization assessment showed normal hybridization patterns for the C-MYC and CCND1 loci; CCND1 RNA overexpression was detected by real-time polymerase chain reaction analysis. Genetic evaluation of this rare condition may be useful in determining if epithelioid sarcoma is associated with a distinct genetic background.


Subject(s)
Chromosome Aberrations , Sarcoma/genetics , Adult , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Humans , In Situ Hybridization, Fluorescence , Male , Polymerase Chain Reaction , Sarcoma/drug therapy
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