12岁患者原发性乳腺瘤的高层次无区别多形性肉瘤:病例报告

IF 0.3 Q4 OBSTETRICS & GYNECOLOGY
Daniela María Cuadrado Franco, Sandra Milena Pantoja Burbano, Natalia Restrepo Abisambra
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引用次数: 0

摘要

乳腺高级别未分化多形性肉瘤(UPS)在儿童中极为罕见,占乳腺恶性肿瘤的不到1%。由于缺乏具体的指导方针,它给诊断和治疗带来了挑战。我们描述的情况下,一个12岁的病人没有明显的病史,谁提出了一个三级保健医院快速增长,疼痛的乳房肿块与皮肤的变化。影像学检查显示一个复杂的BIRADS 4C肿块,无转移迹象。该病例提交给多学科委员会,建议进行初步手术治疗。术后病理报告提示UPS。辅助调强放疗(IMRT)和化疗与异环磷酰胺和多柔比星根据方案适用于儿童非横纹肌肉瘤。患者术后表现良好,移植物完全愈合,无复发迹象。本病例强调了小儿乳腺肉瘤积极手术治疗和个性化辅助治疗的重要性,强调需要进一步的研究来建立具体的治疗指南并优化这一人群的预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sarcoma pleomórfico indiferenciado de alto grado como tumor primario de mama en una paciente de 12 años: reporte de caso
High-grade undifferentiated pleomorphic sarcoma (UPS) of the breast is an extremely rare entity in children, representing less than 1% of malignant breast tumors. It poses a challenge in diagnosis and treatment due to the lack of specific guidelines. We describe the case of a 12-year-old patient with no significant medical history who presented to a tertiary care hospital with a rapidly growing, painful breast mass with cutaneous changes. Imaging studies showed a complex BIRADS 4C mass with no sign of metastasis. The case was submitted to a multidisciplinary board, which indicated primary surgical management. The postoperative pathology report indicated UPS. Adjuvant intensity-modulated radiation therapy (IMRT) and chemotherapy with ifosfamide and doxorubicin were indicated according to the protocol for pediatric non-rhabdomyosarcoma. The patient showed a favorable postoperative outcome, with complete graft healing and no signs of relapse to date. This case highlights the importance of aggressive surgical management and personalized adjuvant treatment in pediatric breast sarcomas, emphasizing the need for additional studies to establish specific management guidelines and optimize outcomes in this population.
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来源期刊
Revista de Senologia y Patologia Mamaria
Revista de Senologia y Patologia Mamaria Medicine-Obstetrics and Gynecology
CiteScore
0.30
自引率
0.00%
发文量
74
审稿时长
63 days
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