An insight into the inferior vena cava leiomyosarcoma

Bhupinder Singla, A. Bansal
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Abstract

Primary vascular leiomyosarcoma (LMS) is a rare tumor accounting for 2% of all LMSs, with the most common site being inferior vena cava (IVC). Overall prognosis is poor, with a median survival of 2 years only. Definitive treatment strategy has not been defined yet, due to the availability of small case series or reports only. However, extrapolating from the treatment of other sarcomas, definitive surgery followed by adjuvant treatment in the form of radiation and chemotherapy is usually followed. This review article focuses on presentation, diagnostic workup, the treatment options for IVC LMS, and their effect on the outcome, so that optimal management can be planned for individual cases. For this, a literature PubMed/Medline search was performed from January 1995 to December 2013 and reviewed to define the rare presentation of these vascular tumors, diagnostic workup, surgical options and reconstruction methods available, and the indications for the use of adjuvant chemotherapy and radiation.
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下腔静脉平滑肌肉瘤的观察
原发性血管平滑肌肉瘤(LMS)是一种罕见的肿瘤,占所有LMS的2%,最常见的部位是下腔静脉(IVC)。总体预后较差,中位生存期仅为2年。由于只有小病例系列或报告,尚未确定最终的治疗策略。然而,从其他肉瘤的治疗推断,最终手术后通常以放疗和化疗的形式进行辅助治疗。本文综述了下腔静脉LMS的临床表现、诊断检查、治疗方案及其对预后的影响,以便针对个别病例制定最佳治疗方案。为此,我们检索了1995年1月至2013年12月的PubMed/Medline文献,回顾了这些血管肿瘤的罕见表现、诊断检查、手术选择和可用重建方法,以及使用辅助化疗和放疗的适应症。
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