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泌尿生殖系统畸形患者的女性下生殖道癌:36例临床病理分析

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

作者信息

Zong Liju, Wang Wenze, He Yonglan, Cheng Ninghai, Xiang Yang

机构信息

Department of Obstetrics and Gynecology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, 100730, Beijing, China.

Department of Pathology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, 100730, Beijing, China.

出版信息

J Cancer. 2019 Jun 2;10(13):3054-3061. doi: 10.7150/jca.30486. eCollection 2019.

Abstract

: 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. : 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. : 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% <0.001). Compared with patients with SCC, patients with adenocarcinoma presented at a younger age (36.1 vs. 47.0 years, =0.011), had more advanced stages disease (57.7% vs. 10.0% were in stage II-IV, =0.022), and tended to have poorer five-year overall survival rates (75.6% vs. 100.0%, =0.279). : 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.

摘要

与泌尿生殖系统畸形并存的下生殖道癌较为罕见。本研究旨在探讨这种罕见的联合病症患者的临床病理特征及预后情况。本研究旨在调查这些患者的临床病理特征及预后,以分析这种罕见病症中临床病理特征之间的关联。对1995年1月至2017年12月在北京协和医院(中国北京)接受治疗的下生殖道癌合并生殖道畸形患者的病历进行回顾性分析,并进行全面的文献综述。采用Fisher精确检验确定变量之间的相关性。共纳入36例患者,其中22例为宫颈癌,10例为阴道癌,2例为宫颈和阴道双原发癌。最常见的生殖道畸形是双子宫(n = 17),63.9%的患者合并泌尿系统畸形。25例(69.4%)为病理确诊的腺癌,10例(27.8%)为鳞状细胞癌(SCC),1例为腺鳞癌。合并泌尿系统畸形的患者腺癌发生率高于未合并畸形的患者(95.7%对30.8%,<0.001)。与SCC患者相比,腺癌患者发病年龄较轻(36.1岁对47.0岁,P = 0.011),疾病分期更晚(57.7%对10.0%为II-IV期,P = 0.022),且五年总生存率较低(75.6%对100.0%,P = 0.279)。同时存在生殖和泌尿系统畸形的患者发生腺癌的可能性较高。建议对有生殖道畸形的女性定期进行严格的妇科检查,包括巴氏涂片和影像学分析,因为她们可能有发生生殖道恶性肿瘤的风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c14/6590040/84ef1f2ed21f/jcav10p3054g001.jpg

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