乳腺原发性血管肉瘤的放疗1例报告

IF 0.9 Q3 MEDICINE, GENERAL & INTERNAL
Yoke Surpri Marlina, Rima Novirianthy, Teuku M. Yus
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引用次数: 1

摘要

背景:原发性乳腺血管肉瘤是一种非常罕见的乳腺恶性肿瘤。它可能有一个潜伏的临床发病,表现为无痛的,通常是离散的可触及的肿块,迅速增长。发病年龄范围为20-50岁。病例描述:我们报告一例年轻女性与可触及和无痛肿块她的左乳房。根据x线摄影和MRI检查的影像学表现,报告为左乳房恶性肿块,怀疑为血管肉瘤。术后病理证实报告一分化良好的血管肉瘤,主要发生在左乳房。患者行单纯乳房切除术后全乳放疗。体外放射治疗采用3DCRT配合FIF技术,规定剂量60Gy,分30次,6周内给予。结论:原发性乳腺血管肉瘤尚无标准治疗方法。乳房切除术仍然是主要的治疗方法。辅助放疗似乎可以改善局部控制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Radiotherapy for primary angiosarcoma of the breast: a case report
Background: Primary breast angiosarcomas are very rare type malignant breast tumor. It may have an insidious clinical onset, presenting as a painless, often discrete palpable mass that grows rapidly. The ranged age of disease is 20-50 years. Case description: We report a case of a young woman with palpable and painless mass of her left breast.  Based on radiological findings with mammography and MRI examination reported as malignant mass of the left breast suspected angiosarcoma. Pathological confirmation post-surgery reported a well-differentiated angiosarcoma that arose primarily in the left breast. Patient treated with simple mastectomy followed by whole breast radiotherapy. External beam radiotherapy delivered using 3DCRT with FIF technique, prescribed dose 60Gy in 30 fractions within 6 weeks. Conclusion: There is no established standard treatment for primary angiosarcoma of the breast. Mastectomy remains the mainstay of treatment. Adjuvant radiotherapy appears to improve local control.
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来源期刊
Bali Medical Journal
Bali Medical Journal MEDICINE, GENERAL & INTERNAL-
自引率
50.00%
发文量
8
审稿时长
3 weeks
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