Suppr超能文献

肺泡软组织肉瘤。半个世纪的临床病理研究。

Alveolar soft-part sarcoma. A clinico-pathologic study of half a century.

作者信息

Lieberman P H, Brennan M F, Kimmel M, Erlandson R A, Garin-Chesa P, Flehinger B Y

机构信息

Department of Pathology, Memorial Sloan-Kettering Cancer Center, New York.

出版信息

Cancer. 1989 Jan 1;63(1):1-13. doi: 10.1002/1097-0142(19890101)63:1<1::aid-cncr2820630102>3.0.co;2-e.

Abstract

In the period from 1923 to 1986 our pathologists examined pathologic material from 102 patients with alveolar soft-part sarcoma (ASPS). Followup clinical data is available for 91. Median followup is 7 years (range 1 month to 27 years). Local recurrence was only found if residual disease was left at the time of the original excision. Survival in those patients who presented without metastases was 77% at 2 years, 60% at 5 years, 38% at 10 years and 15% at 20 years (median 6 years). No survival advantage could be demonstrated for patients who received chemo and/or radiotherapy, although numbers are small and staging not uniform. An evaluation by electron microscopy and immunohistochemistry cannot confirm recent claims that ASPS is a muscle tumor. ASPS is an unusual neoplasm; the primary therapeutic option is aggressive surgical excision. Survival even with the development of metastases can be long.

摘要

在1923年至1986年期间,我们的病理学家检查了102例肺泡软组织肉瘤(ASPS)患者的病理材料。91例患者有随访临床数据。中位随访时间为7年(范围1个月至27年)。仅在初次切除时残留疾病的情况下才发现局部复发。无转移患者的2年生存率为77%,5年生存率为60%,10年生存率为38%,20年生存率为15%(中位生存时间6年)。尽管病例数少且分期不统一,但接受化疗和/或放疗的患者未显示出生存优势。通过电子显微镜和免疫组织化学评估无法证实最近关于ASPS是一种肌肉肿瘤的说法。ASPS是一种不常见的肿瘤;主要的治疗选择是积极的手术切除。即使发生转移,生存期也可能很长。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验