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Carcinoma of the lower female genital tract in patients with genitourinary malformations: a clinicopathologic analysis of 36 cases

机译:泌尿生殖系统畸形女性下生殖道癌36例临床病理分析

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摘要

>Background: Lower genital tract carcinomas that coexist with genitourinary malformations are rare. The aim of this study was to investigate the clinicopathologic characteristics and outcomes of patients with this rare joint condition. The aim of this study was to investigate the clinicopathologic characteristics and outcomes of these patients to analyze the associations among clinicopathologic features in this rare entity.>Methods: The medical records of patients with carcinoma of lower genital tract combined with genital tract malformations who were treated at Peking Union Medical College Hospital (Beijing, China) between January 1995 and December 2017 were retrospectively reviewed and a comprehensive literature review was performed. The correlations between variables were determined using Fisher's exact test.>Results: Thirty-six patients were identified, among whom 22 had cervical carcinoma, 10 had vaginal carcinoma, and two had carcinomas of both the cervix and vagina. The most common genital tract anomaly was uterus didelphys (n=17), and 63.9% of patients had with urinary tract malformations. Twenty-five (69.4%) had pathologically confirmed adenocarcinoma, 10 (27.8%) had squamous cell carcinoma (SCC), and 1 had adenosquamous carcinoma. Patients with urinary tract malformations developed adenocarcinoma more frequently than those without malformations (95.7% vs. 30.8% P<0.001). Compared with patients with SCC, patients with adenocarcinoma presented at a younger age (36.1 vs. 47.0 years, P=0.011), had more advanced stages disease (57.7% vs. 10.0% were in stage II-IV, P=0.022), and tended to have poorer five-year overall survival rates (75.6% vs. 100.0%, P=0.279).>Conclusions: Patients with simultaneous malformations of the genital and urinary tracts had a high probability of developing adenocarcinoma. It is recommended that rigorous gynecologic exams with Pap smears and imaging analyses be performed periodically in women with genital malformations, as they may be at a risk of genital malignancies.
机译:>背景:与泌尿生殖系统畸形并存的下生殖道癌很少见。这项研究的目的是调查这种罕见关节疾病患者的临床病理特征和预后。这项研究的目的是调查这些患者的临床病理特征和结局,以分析这一罕见实体的临床病理特征之间的关联。>方法:下生殖道癌合并肝癌的病历回顾性分析1995年1月至2017年12月在北京协和医院(中国北京)治疗的生殖道畸形,并进行了全面的文献综述。使用Fisher精确检验确定变量之间的相关性。>结果:共鉴定出36例患者,其中宫颈癌22例,阴道癌10例,宫颈和阴道癌2例。生殖道异常最常见的是子宫双侧子宫(n = 17),有63.9%的患者患有尿路畸形。病理证实的腺癌中有25例(69.4%),鳞状细胞癌(SCC)有10例(27.8%),腺鳞癌1例。尿路畸形患者比无畸形患者更容易发生腺癌(95.7%vs. 30.8%P <0.001)。与SCC患者相比,年龄较小的腺癌患者(36.1岁对47.0岁,P = 0.011),病情更严重(II-IV期为57.7%,10.0%,P = 0.022),并且倾向于较低的五年总生存率(75.6%对100.0%,P = 0.279)。 。建议对有生殖器畸形的妇女定期进行严格的妇科检查,包括子宫颈抹片检查和影像学检查,因为它们可能有生殖器恶性肿瘤的风险。

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