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上皮样肉瘤临床诊治分析 被引量:3

Clinical analysis on diagnosis and treatment of epithelioid sarcoma
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摘要 背景与目的:上皮样肉瘤是一种少见的软组织肉瘤,多表现为肢体远端的结节或溃疡性病变,可通过腱鞘局部播散、淋巴道和血道转移。因其切除后易复发转移、有较高的淋巴结转移率而区别于其他的软组织肉瘤。本文通过分析上皮样肉瘤临床特点,治疗效果,生存情况,预后因素,旨在探讨其治疗方法及预后的影响因素等。方法:回顾我院1999-2007年收治的获得随访的18例上皮样肉瘤,对其临床表现、淋巴结转移、治疗情况、生存率及预后进行分析。结果:上皮样肉瘤5年生存率为41%,局部复发率为44.4%。即使截肢,术后仍有复发。在11例行淋巴结清扫的患者中淋巴结转移率为63.6%。结论:上皮样肉瘤是一种侵袭性较强、淋巴结转移率高、术后易复发的软组织肉瘤,手术应充分考虑切除的广泛性。 Background and purpose: Epithelioid sarcoma is a rare histological subtype of sarcoma. The tumor frequently appears as a nodular or ulcerated lesion on a distal extremity. This tumor can extend regionally along tendon sheaths and spread through lymphatics and vascular channels. The high local recurrence rate and incidence of nodal metastases differ epithelioid sarcoma from other types of sarcoma. The aim of this study was to evaluate treatment and prognostic factors of epithellold sarcoma. Methods: The clinical manifestation, lymph node metastasis, treatment, survival rate, prognosis of 18 cases of the epithelioid sarcoma in limbs were reviewed. All 18 cases were treated and followed up in our hospital from 1999 to 2007. Results: The 5-year survival rate was 70% . The local recurrence rate was 44.4%. The lymph node metastasis rate was 63.6% in 11 cases who had been treated with lymphadenectomy. Conclusions: Epithelioid sarcoma is a very aggressive form of soft-tissue sarcoma, with high rates of local recurrence and a propensity to lymph node metastases. Extensive resection should be fully considered during operation.
出处 《中国癌症杂志》 CAS CSCD 2008年第1期11-14,共4页 China Oncology
关键词 上皮样肉瘤 软组织肉瘤 诊断 预后 epithelioid sarcoma soft tissue sarcomas diagnosis prognosis
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参考文献13

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同被引文献18

  • 1郭阳,田光磊,胡溱,常万绅,李淳.上皮样肉瘤的症状和治疗[J].中华手外科杂志,2004,20(4):208-209. 被引量:9
  • 2刘秀美,程秀英.上皮样肉瘤的病理诊断与鉴别诊断[J].中国骨肿瘤骨病,2006,5(6):364-366. 被引量:7
  • 3徐立斌,于胜吉,邵永孚,张宏图,赵振国.上皮样肉瘤14例临床分析[J].癌症,2007,26(7):782-784. 被引量:8
  • 4ChristopherDM,FletcherK,UnniK,et al.世界卫生组织肿瘤分类及诊断标准系列:软组织与骨肿瘤病理学和遗传学[M].程虹等译,北京:人民卫生出版社,2006.237-241.
  • 5Guillnu L, Wadden C, Coindre JM,et al. Proximal-type epithelioid sarcoma: a distinctive aggressive neoplams showing rhabdoid features. Clinicopathologic, immunohistochemical, and ultrastructural study of a series [ J ]. Am J Surg Pathol, 1997,21 (2) :130 -146.
  • 6Rekhi B, Gorad BD, Chinoy RF. Proximal-type epithelioid sarcoma--a rare, aggressive subtype of epithelioid sarcoma presenting as a recurrent perineal mass in a middle-aged male [ J ]. World J Surg Onco1,2007,6 (5) :28.
  • 7Izunfi T, Oda Y, Hasegawa T, et al. Prognostic significance of dysadherin expression in epithelioid sarcoma and its diagnostic utility in distinguishing epithelioid sarcoma from malignant rhabdoid tumor[ J]. Mod Pathol,2006,19(6 ) :820 - 831.
  • 8Narendra H,Ray S, Rao L, et al. Malignant extrarenal rhabdoid tumor of the vulva an adult. [ J]. J Cancer Res Ther, 2010,6 (1) :82 -85.
  • 9李黎,岑石强,黄富国,张世琼,屠重琪.11例上皮样肉瘤临床治疗分析[J].中国修复重建外科杂志,2007,21(12):1315-1318. 被引量:4
  • 10范宜娟,杨滢瑜,陈荣,章林培.近端型上皮样肉瘤3例临床病理分析[J].现代肿瘤医学,2009,17(5):938-941. 被引量:2

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