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Low grade endometrial stromal sarcoma with epithelial differentiation mimicking endometriosis

机译:低级子宫内膜基质肉瘤,上皮分化模仿子宫内膜异位症

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摘要

Low grade endometrial stromal sarcoma (ESS) is a difficult diagnostic entity as the tumour cells closely resemble normal endometrial stromal cells with minimal nuclear atypia and mitotic activity. The site of occurrence in the uterine corpus is a useful suggestion for this tumour type, but when present at extrauterine sites it may be difficult to diagnose. In addition, a variant with epithelial differentiation has been recently described which mimics both endometriosis and low grade adenosarcoma. We describe the case of a 52-year-old female who presented with a pelvic tumour showing very minimal cytological atypia mimicking endometriosis, but diagnosed as low grade ESS with epithelial differentiation. We also discuss the possible role of a characteristic translocation t(7;17)(pl5;q21), resulting in the fusion of the JAZF1/JJAZ1 genes, in aiding the histological diagnosis.
机译:低级子宫内膜基质肉瘤(ESS)是一种难以诊断的实体,因为肿瘤细胞与最小核原型和有丝分裂活性相似的正常子宫内膜基质细胞。 子宫毒物的发生位点是对这种肿瘤类型的有用建议,但是当存在于Impertuterine位点时,可能难以诊断。 此外,最近已经描述了具有上皮分化的变体,其模仿子宫内膜异位症和低等级的腺肉瘤。 我们描述了一个患有盆腔肿瘤的52岁女性的案例,显示出非常微观的细胞学类别模仿子宫内膜异位症,但被诊断为具有上皮分化的低等级。 我们还讨论了特征易位T(7; 17)(PL5; Q21)的可能作用,导致Jazf1 / Jjaz1基因的融合,以促进组织学诊断。

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