Liang Dongni, Li Lei, He Yanmei, Jiang Wei
Department of Pathology, West China Second University Hospital, Sichuan University; Key Laboratory of Birth Defects and Related Diseases of Women and Children (Sichuan University), Ministry of Education, China.
Indian J Pathol Microbiol. 2020 Feb;63(Supplement):S94-S97. doi: 10.4103/IJPM.IJPM_269_19.
Primary uterine angiosarcoma is a very rare malignant tumor in the female genital tract and only 23 cases have been previously reported in the literature. It is often clinically misrecognized as another disease due to its low incidence. In this report, we present a new case of a 78-year-old woman diagnosed on histopathologic observation and immunohistochemical staining. Additionally, available studies are collected and reviewed to summarize the clinical and pathological characteristics of primary uterine angiosarcoma to remind gynecologists and pathologists of this rare disease when they encounter such cases.
原发性子宫血管肉瘤是女性生殖道中一种非常罕见的恶性肿瘤,此前文献中仅报道过23例。由于其发病率低,临床上常被误诊为其他疾病。在本报告中,我们介绍了一例78岁女性的新病例,该病例经组织病理学观察和免疫组化染色确诊。此外,收集并回顾了现有研究,以总结原发性子宫血管肉瘤的临床和病理特征,提醒妇科医生和病理学家在遇到此类病例时注意这种罕见疾病。