免疫治疗和精确肿瘤学中的影像:脾和肝血管肉瘤。

Q3 Medicine
Anagha Deshpande, Javier Munoz, Katalin Kelemen, Vrushali Dabak, Amr Hanbali, Razelle Kurzrock
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引用次数: 0

摘要

原发性脾或肝血管肉瘤是一种极为罕见且侵袭性的恶性肿瘤,预后差。主要的治疗方法是手术切除和化疗。我们报告一个50岁女性血管肉瘤的病例,她表现为瘀伤、疲劳、瘀斑和肝脾肿大。多激酶抑制剂舒尼替尼治疗4周后出现脾出血并死亡。最近的研究表明免疫疗法对血管肉瘤有临床益处。此外,测序技术已经显示了血管肉瘤中涉及的各种分子畸变,这为精确匹配的靶向治疗提供了机会,例如VEGF/VEGFR轴和PI3K/Akt/mTor通路的抑制剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Images in Immunotherapy and Precision Oncology: Angiosarcoma of the Spleen and Liver.

Images in Immunotherapy and Precision Oncology: Angiosarcoma of the Spleen and Liver.

Images in Immunotherapy and Precision Oncology: Angiosarcoma of the Spleen and Liver.

Primary splenic or hepatic angiosarcomas are ultra-rare and aggressive malignancies associated with poor prognosis. The mainstay treatments are surgical resection and chemotherapy. We report a case of angiosarcoma in a 50-year-old woman who presented with bruising, fatigue, ecchymosis, and hepatosplenomegaly. She was treated with the multi-kinase inhibitor sunitinib for 4 weeks before developing a splenic hemorrhage and succumbing. Recent studies have demonstrated the clinical benefit of immunotherapies in angiosarcomas. Additionally, sequencing techniques have showcased the diverse molecular aberrations involved in angiosarcomas, which offer opportunities for precision-matched targeted therapies such as inhibitors of the VEGF/VEGFR axis and PI3K/Akt/mTor pathway.

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CiteScore
2.40
自引率
0.00%
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