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Primary oral leiomyosarcoma: A systematic review and update

机译:原代口腔Leiomyosarcoma:系统审查和更新

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Abstract The aim of this systematic review was to address the clinicopathologic inconsistencies noted with primary oral leiomyosarcoma in the literature by amassing the available data published into a comprehensive analysis. Eligibility criteria included publications of cases with dedicated immunohistochemical work‐up along with radiographs to evaluate location. Based on these criteria, the systematic review compiled 29 cases. Four primary location sites were identified in the reported cases: soft tissue presentation only, soft tissue with bony involvement, bony involvement only, and bony involvement with a soft tissue component. The majority of primary oral leiomyosarcoma cases reviewed showed a soft tissue predilection, which is in contrast to prior reports of jawbones being the most common site. In addition, there was an improved 5‐year survival rate for primary oral leiomyosarcoma limited to the oral cavity and gnathic bones without extension into paranasal sinuses.
机译:摘要这种系统评价的目的是通过减少公布的综合分析,解决文学中原发性口腔肌肉肉瘤中的临床病理学不一致。 资格标准包括具有专用免疫组织化学处理的案件的出版物以及X线仪评估位置。 根据这些标准,系统评价已编制29例。 在报告的病例中确定了四个主要位置位点:软组织呈现,软组织与骨骼参与,仅骨骼受累,骨骼参与和骨骼参与软组织成分。 综述大多数原发性口腔肌肉蛋白酶病例显示出软组织偏移,与Jawbones是最常见的网站的先前报告相反。 此外,对原发性口腔Leiomyosarcoma有限的5年生存率限于口腔和粪便骨骼,没有延伸到副血管鼻窦中。

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