Department of Obstetrics and Gynecology, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia.
Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia.
Niger Postgrad Med J. 2022 Apr-Jun;29(2):116-122. doi: 10.4103/npmj.npmj_733_21.
To report a single-center experience in non-epithelial malignant ovarian tumours (NEMOT), by presenting different clinical and pathological characteristics, management and outcomes.
We retrospectively reviewed electronic files of all female patients who underwent surgery for NEMOT at the Gynecology Department of King Abdulaziz University Hospital, Jeddah, Saudi Arabia, from July 2003 to July 2019. We collected baseline demographic, anthropomorphic and clinical data; pathological characteristics; management and follow-up data; and outcomes including residual disease, recurrence and last follow-up status (deceased or alive).
Thirty-three women were included; mean (standard deviation) age = 33.24 (17.72) years, range = 4, 86 years. Granulosa cell tumor was the most frequent subtype diagnosed in 17 (51.5%) patients, followed by germ cell tumours 13 (39.4%). The majority of patients were diagnosed at FIGO Stage I (22, 66.7%) and with tumor Grade 1 (23, 69.7%), while 8 (24.2%) were diagnosed with Grade 3 tumors. Granulosa cell and Sertoli-Leydig cell tumours were diagnosed at an older age (mean age = 39.30 vs. 23.92 years) compared to germ cell tumours, respectively (P = 0.012). Two-third of the patients benefited from conservative surgery including oophorectomy + staging, and 16 (48.5%) benefited from chemotherapy with bleomycin, etoposide and platinum being the most common protocol (13, 39.4%) for germ cell tumours. Postoperatively, only 2 (6.1%) patients had residual disease. Recurrence and mortality were reported in one and four patients, respectively, resulting in recurrence rate = 3.0% (95% confidence interval [CI] = 0.01%, 15.8%) and mortality rate = 12.1% (95% CI = 3.4%, 28.2%).
The present series of NEMOT was predominated by sex cord-stromal cell tumors, which were diagnosed in patients with older age, while germ cell tumours were underrepresented. Although survival rates were comparable to those reported internationally, more consideration should be given to following up patients regarding fertility outcomes to provide a more comprehensive evaluation of treatment success and quality of care.
报告单一中心非上皮性卵巢恶性肿瘤(NEMOT)的经验,介绍不同的临床和病理特征、治疗方法和结局。
我们回顾性分析了 2003 年 7 月至 2019 年 7 月在沙特阿拉伯吉达阿卜杜勒阿齐兹国王大学医院妇科接受手术治疗 NEMOT 的所有女性患者的电子病历。我们收集了基线人口统计学、人体测量学和临床数据;病理特征;管理和随访数据;以及包括残留疾病、复发和最后随访状态(死亡或存活)在内的结局。
共纳入 33 名女性患者;平均(标准差)年龄为 33.24(17.72)岁,范围为 4-86 岁。颗粒细胞瘤在 17 名(51.5%)患者中最常见,其次是生殖细胞肿瘤 13 名(39.4%)。大多数患者诊断为国际妇产科联合会(FIGO)Ⅰ期(22 名,66.7%),肿瘤分级为 1 级(23 名,69.7%),而 8 名(24.2%)诊断为 3 级肿瘤。颗粒细胞瘤和 Sertoli-Leydig 细胞瘤的诊断年龄较生殖细胞肿瘤大(平均年龄分别为 39.30 岁和 23.92 岁)(P=0.012)。三分之二的患者接受了保留卵巢的手术治疗,包括卵巢切除术+分期手术,16 名(48.5%)患者接受了化疗,博来霉素、依托泊苷和顺铂联合化疗是生殖细胞肿瘤最常见的方案(13 名,39.4%)。术后仅 2 名(6.1%)患者有残留疾病。1 名和 4 名患者分别出现复发和死亡,复发率为 3.0%(95%置信区间[CI]:0.01%,15.8%),死亡率为 12.1%(95%CI:3.4%,28.2%)。
本系列非上皮性卵巢恶性肿瘤以性索-间质细胞肿瘤为主,这些肿瘤发生在年龄较大的患者中,而生殖细胞肿瘤则相对少见。尽管生存率与国际报道相似,但应更多地关注患者的生育结局,以提供对治疗成功和护理质量的更全面评估。