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A Rare Case of Poorly-Differentiated Sertoli Leydig Cell Tumour of Ovary with Mesenchymal Heterology

机译:少见的间质异位性卵巢Sertoli Leydig细胞瘤罕见病例

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Sertoli?Leydig Cell Tumours (SLCT) accounts for less than 0.5% of all ovarian neoplasms. Presence of mesenchymal heterologous elements in a poorly differentiated SLCT is extremely uncommon. It not only causes diagnostic difficulty but also renders an aggressive behaviour to the tumour. We report a rare case of poorly differentiated SLCT with cartilage and rhabdomyoblastic differentiation along with review of literature.
机译:Sertoli?Leydig细胞肿瘤(SLCT)占所有卵巢肿瘤的不到0.5%。分化差的SLCT中存在间充质异源元件极为罕见。它不仅造成诊断困难,而且使肿瘤表现出侵略性。我们报道了少见的SLCT分化差的病例,伴有软骨和横纹母细胞分化,并有文献复习。

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