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Clinical Characteristics and Prognostic Factors of Small Intestine Angiosarcoma: a Retrospective Clinical Analysis of 66 Cases

机译:小肠血管肉瘤的临床特点及预后因素:回顾性临床分析66例

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>Background/Aims: Primary angiosarcoma of the small intestine is a rare neoplasia, and there are limited data from systematic analyses. The aim of this study is to describe the clinical and pathological characteristics in addition to the prognostic factors for this rare neoplasia. Methods: We retrospectively collected the clinical records and prognostic information of 66 patients with small intestine angiosarcoma reported between 1970 and 2017. We used the Chi-square test, the log-rank test, and Cox regression analyses to evaluate the data. Results: There were 66 patients diagnosed with small intestine angiosarcoma. The onset age ranged from 24-92 years old. There were 24 patients diagnosed before the year 2000, and 42 patients were diagnosed after 2000. The data indicated that 49 cases were diagnosed as primary disease, and the remaining 15 cases were secondary disease. The main clinical symptoms were nonspecific and included gastrointestinal (GI) bleeding and abdominal pain. Additionally, we found multi-center foci were one of the characteristics of this disease. Radiation-induced small intestine angiosarcoma (RSIA) is a special type of disease with a similar prognosis. This type was more frequent in females and decreased after the year 2000. We also found that GI bleeding was less common in RSIA cases. The log-rank test results revealed that old-age, poor differentiation, and GI bleeding were associated with worse prognosis. Surgical treatment showed a trend toward a prolonged survival time. However, the result was not statistically significant. Our results show treatment with adjuvant therapy improved prognosis. The multivariate Cox analysis demonstrated adjuvant therapy was an independent indicator of a favorable outcome in small intestine angiosarcoma patients. Conclusion: Pay attention to the unexplained gastrointestinal bleeding could lead to a faster diagnosis and control of small intestine angiosarcoma. Furthermore, treatments including adjuvant therapy can effectively improve the prognosis.
机译:> 背景/目的: 小肠原发性血管肉瘤是一种罕见的瘤形成,并且系统分析的数据有限。这项研究的目的是描述这种罕见瘤形成的临床和病理特征以及预后因素。 方法: 我们回顾性收集了1970年至2017年间报告的66例小肠血管肉瘤患者的临床记录和预后信息。我们采用卡方检验,对数秩测试和Cox回归分析以评估数据。 结果: 有66例被诊断出患有小肠血管肉瘤的患者。发病年龄为24-92岁。 2000年以前诊断为24例,2000年以后诊断为42例。数据表明,诊断为原发疾病的有49例,其余为继发性的15例。主要临床症状是非特异性的,包括胃肠道(GI)出血和腹痛。此外,我们发现多中心病灶是该疾病的特征之一。辐射诱发的小肠血管肉瘤(RSIA)是一种预后相似的特殊疾病。这种类型在女性中更为常见,并且在2000年以后有所减少。我们还发现在RSIA病例中胃肠道出血较少见。对数秩检验结果表明,老年人,分化差和胃肠道出血与预后差有关。手术治疗显示出生存时间延长的趋势。但是,结果在统计上并不显着。我们的结果表明,辅助治疗可以改善预后。多元Cox分析表明,辅助治疗是小肠血管肉瘤患者预后良好的独立指标。 结论: 注意无法解释的胃肠道出血可能导致小肠血管肉瘤的更快诊断和控制。此外,包括辅助疗法在内的治疗可以有效改善预后。

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