Immune Cell

免疫细胞
  • 文章类型: Case Reports
    原发性乳腺血管肉瘤是一种极其罕见的疾病,预后不良。原发性血管肉瘤与继发性血管肉瘤不同,通常发生在以前接受过乳腺癌治疗的患者身上。原发性乳腺血管肉瘤的低发病率阻碍了其病因和潜在治疗方法的阐明。这里,我们报道了一例原发性乳腺血管肉瘤患者,该患者在手术后复发。肿瘤对全身治疗是难治的,患者在手术后18个月死亡。我们使用RNA测序进行肿瘤的基因表达谱分析。高肿瘤炎症特征评分表明免疫相关信号的富集。CIBERSORTx,用于基于基因表达表征复杂组织的细胞组成的工具,表明肿瘤中的免疫细胞主要是巨噬细胞,使用免疫组织化学分析证实了这一点。这些发现表明可能使用检查点免疫疗法治疗原发性乳腺血管肉瘤。
    Primary breast angiosarcoma is an extremely rare disease with a poor prognosis. Primary angiosarcoma is distinct from secondary angiosarcoma, which usually occurs in patients who have been previously treated for breast cancer. The low incidence of primary breast angiosarcoma has hindered the elucidation of its etiology and potential therapies. Here, we report a case of a patient with primary breast angiosarcoma who experienced recurrence after surgery. The tumor was refractory to systemic treatments, and the patient died 18 months after the surgery. We used RNA sequencing for gene expression profiling of the tumor. A high tumor inflammation signature score indicated enrichment in immune-related signaling. CIBERSORTx, a tool used to characterize the cellular composition of complex tissues based on gene expression, indicated that the immune cells in the tumor were predominantly macrophages, and this was confirmed using immunohistochemical analysis. These findings indicate the possible use of checkpoint immunotherapy for the treatment of primary breast angiosarcoma.
    导出

    更多引用

    收藏

    翻译标题摘要

    我要上传

       PDF(Pubmed)

公众号