罕见的原发性乳腺血管肉瘤伴骨转移:病例报告

Rupita Sari, Kiki A. Rizki, A. Yantisetiasti
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引用次数: 0

摘要

背景:血管肉瘤是一种源自内皮细胞的罕见侵袭性恶性肿瘤。原发性乳腺血管肉瘤(PBA)极为罕见,在所有乳腺恶性肿瘤中占比不到 1%。原发性乳腺血管肉瘤的骨转移更为罕见,因此是一种独特的临床实体。病例介绍:我们介绍了一名 37 岁女性的病例,她最初因乳房肿块迅速增大而就诊。活组织检查确诊为 PBA,她接受了改良根治性乳房切除术,随后接受了放疗。17 个月后,她出现了进行性下肢无力、大小便失禁等症状。影像学检查发现,Th4-Th6水平有一个脊柱转移瘤。活检和免疫组化证实了转移性血管肉瘤。患者接受了椎板切除术和后路稳定术。结论:该病例凸显了伴有骨转移的 PBA 的罕见性和侵袭性。它强调了早期发现、综合治疗和长期监测对治疗这种具有挑战性疾病的重要性。要了解 PBA 伴骨转移的潜在机制并制定有效的治疗策略,还需要进一步的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Rare Primary Breast Angiosarcoma with Bone Metastasis: A Case Report
Background: Angiosarcoma is a rare and aggressive malignant tumor originating from endothelial cells. Primary breast angiosarcoma (PBA) is exceedingly uncommon, accounting for less than 1% of all breast malignancies. Bone metastasis from PBA is even rarer, making it a unique clinical entity. Case presentation: We present the case of a 37-year-old woman who initially presented with a rapidly enlarging breast mass. A biopsy confirmed the diagnosis of PBA, and she underwent a modified radical mastectomy followed by radiotherapy. Seventeen months later, she developed progressive lower extremity weakness and urinary and bowel incontinence. Imaging revealed a spinal metastasis at the Th4-Th6 level. Biopsy and immunohistochemistry confirmed metastatic angiosarcoma. The patient underwent laminectomy and posterior stabilization. Conclusion: This case highlights the rarity and aggressive nature of PBA with bone metastasis. It emphasizes the importance of early detection, comprehensive treatment, and long-term surveillance in managing this challenging disease. Further research is needed to understand the underlying mechanisms and develop effective therapeutic strategies for PBA with bone metastasis.
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