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首页> 外文期刊>Anticancer Research: International Journal of Cancer Research and Treatment >Primary Angiosarcoma of the Kidney: Literature Review of a Rare Nosologic Entity
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Primary Angiosarcoma of the Kidney: Literature Review of a Rare Nosologic Entity

机译：肾脏的原发性昂贵arcoma：稀有臭味实体的文献综述

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摘要

Primary angiosarcoma of the kidney is a rare tumor, hence little is known concerning its diagnostic features and therapeutic management. We conducted this survey to present a complete literature review with emphasis on clinicopathological features, diagnosis and therapy. A thorough search was conducted in MEDLINE/PubMed. All relevant studies concerning primary renal angiosarcomas in adults were thoroughly reviewed. Primary renal angiosarcoma is characterized by an overall poor prognosis, is of unknown etiology and occurs most commonly in males between 60 and 70 years old. Presence of distant metastasis at the time of diagnosis is prevalent. Histopathological examination and immunohistochemical studies are the most important diagnostic tools. Treatment options include surgery, chemotherapy, radiotherapy and immunotherapy. Conclusion: Primary renal angiosarcoma is a rare but aggressive malignancy with low response to available therapeutic regimens and dismal survival rates.
机译：肾脏的原发性肾炎是一种罕见的肿瘤，因此熟知其诊断特征和治疗管理几乎不少。 我们进行了本调查，以重点对临床病理特征，诊断和治疗的重点进行了完整的文献综述。 在Medline / Pubmed中进行了彻底搜索。 彻底审查了关于成人原发性肾上腺癌的所有相关研究。 原发性肾上血管征达的特点是预后的总体差，属于未知的病因，最常见于60至70岁的男性。 诊断时的远距离转移是普遍存在的。 组织病理学检查和免疫组化研究是最重要的诊断工具。 治疗方案包括手术，化疗，放疗和免疫疗法。 结论：原发性肾癌症是一种罕见但积极的恶性肿瘤，对可用治疗方案和惨淡的存活率低。

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