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Radiological Appearance of Primary Ovarian Angiosarcoma in a 79-Year-Old Woman: a case report and literature review

机译:79岁女性原发性卵巢血管肉瘤的放射学表现:一例病例并文献复习

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摘要

Primary ovarian angiosarcoma is an extremely rare disease. Most reports concern young premenopausal patients, and relatively few case reports regarding elderly patients exist [1]. In this report, we present a case of ovarian angiosarcoma in a 79-year-old woman. The patient's initial chief complaint was abdominal distention. Sonography, computed tomography (CT), and magnetic resonance imaging (MRI) demonstrated a large heterogeneous mass with hemorrhaging, solid compartmentalization, and an abundant vascular network. The diagnosis of primary ovarian angiosarcoma was verified using immunohistochemistry staining with CD34, CD31, and Fli-1. In this report, we describe the sonographic, CT, and MRI features of this case of angiosarcoma.
机译:原发性卵巢血管肉瘤是一种极为罕见的疾病。大多数报道涉及绝经前的年轻患者,而关于老年患者的病例报道则相对较少[1]。在本报告中,我们介绍了一名79岁妇女的卵巢血管肉瘤病例。病人最初的主要主诉是腹胀。超声检查,计算机断层扫描(CT)和磁共振成像(MRI)表现出较大的异质性肿块,并伴有出血,固体分隔和丰富的血管网络。使用CD34,CD31和Fli-1的免疫组织化学染色验证了原发性卵巢血管肉瘤的诊断。在本报告中,我们描述了此例血管肉瘤的超声,CT和MRI特征。

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