Regular ArticleCytogenetics of Uterine Sarcomas: Presentation of Eight New Cases and Review of the Literature☆
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Chapter 20 - Uterine Mesenchymal Tumors
2017, Diagnostic Gynecologic and Obstetric PathologyGenomic characterization of endometrial stromal sarcomas with array comparative genomic hybridization
2015, Experimental and Molecular PathologyCitation Excerpt :In previous studies, 27 ESS cases have been analyzed using classical cytogenetics. ESSs were found to be a highly heterogeneous group of tumors, according to these investigations (Amant et al., 2003; Dal Cin et al., 1992; Fletcher et al., 1991; Fresia et al., 1992; Fuzesi et al., 1995; Gil-Benso et al., 1999; Hrynchak et al., 1994; Iliszko et al., 1998; Koontz et al., 2001; Laxman et al., 1993; Micci et al., 2003; Pauwels et al., 1996; Sonobe et al., 1999; Sreekantaiah et al., 1991). In a study by our group in 2005, conventional CGH analysis of low-grade ESS, as well as UES cases has been performed (Halbwedl et al., 2005).
Areas with benign morphologic and immunohistochemical features are associated with some uterine leiomyosarcomas
2007, Gynecologic OncologyCitation Excerpt :The findings of this study suggest that the progression from LM to LMS may be more likely with cellular and symplastic leiomyomata. One recent study has shown rearrangements at chromosome 10q22 in cellular leiomyomata [10] that are also seen in LMS [11]. Rearrangement of 10q22 is seen in only 5% of all uterine leiomyomata [12].
Array comparative genomic hybridization analysis of uterine leiomyosarcoma
2005, Gynecologic Oncology
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This work was supported by Grant 4.PO5A.079.10 from the Polish State Committee for Scientific Research, the Swedish Cancer Society, and the Coleman Leukemia Research Fund.
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To whom correspondence and reprint requests should be addressed at Department of Biology and Genetics, Medical University of Gdańsk, 1 Dębinki St., 80-211 Gdańsk, Poland. Fax:48–58–302–32–76. E-mail:[email protected].