Gao Jinping, Zhang Jintian, Tian Wenyan, Teng Fei, Zhang Huiying, Zhang Xuhong, Wang Yingmei, Xue Fengxia
a Department of Obstetrics and Gynecology , Tianjin Medical University General Hospital , Tianjin , China.
Cancer Biol Ther. 2017 Mar 4;18(3):123-131. doi: 10.1080/15384047.2017.1281495. Epub 2017 Jan 24.
Uterine malformation is a rare deformity in woman, and only a few cases concerning endometrial cancer arising in patients with congenital uterine anomalies have been reported. Herein, we present 3 cases of endometrial cancer with different congenital uterine anomalies, and review studies involving congenital uterine anomalies associated with endometrial cancer in the past 25 years, to identify similarities and differences in clinicopathologic characteristics and prognosis between endometrial cancer associated with uterine anomalies, and normal uterus.
Case 1 was a 75-year-old gravida 1, para 0, woman with carcinosarcoma (mixed well-differentiated endometrial adenocarcinoma and undifferentiated sarcoma) of the right cavity (grade III, and at least stage II ) of a uterus didelphys. The tumor recurred within 7 months after surgery, salvage radiotherapy was unsuccessful; the patient died 8 months after the surgery. Case 2 was a 63-year-old gravida 5, para 3, woman with a bicornuate uterus and uterus papillary serous carcinoma of the right horn (grade III, stage IIIC). She did not respond to the chemotherapy post surgery and died within 4 months. Case 3 was a 60-year-old gravida 0, para 0, woman with a complete septate uterus and an oblique vaginal septum of the upper region of the vagina with endometrioid adenocarchcinoma of the left cavity (grade II, stage IA). No adjuvant therapy was administered and the patient had recovered 2 y after the surgery.
Clinicians should be aware of the coexistence of uterine malignancies and uterine anomalies in patients presenting with persistent abnormal uterine bleeding, but with negative endometrial biopsy or failed in the operation of endometrial biopsy. In such cases, magnetic resonance imaging has an important role in the diagnosis of both malformation and malignancy, and an exploratory laparotomy should be performed to avoid delaying the diagnosis and treatment of cancers.
子宫畸形在女性中是一种罕见的畸形,仅有少数关于先天性子宫异常患者发生子宫内膜癌的病例报道。在此,我们呈现3例伴有不同先天性子宫异常的子宫内膜癌病例,并回顾过去25年中涉及与子宫内膜癌相关的先天性子宫异常的研究,以确定子宫异常相关的子宫内膜癌与正常子宫的子宫内膜癌在临床病理特征和预后方面的异同。
病例1是一名75岁、孕1产0的女性,患有双子宫右腔的癌肉瘤(高分化子宫内膜腺癌与未分化肉瘤混合)(III级,至少II期)。肿瘤在手术后7个月内复发,挽救性放疗未成功;患者在手术后8个月死亡。病例2是一名63岁、孕5产3的女性,患有双角子宫及右角的子宫乳头状浆液性癌(III级,IIIC期)。她术后对化疗无反应,在4个月内死亡。病例3是一名60岁、孕0产0的女性,患有完全纵隔子宫及阴道上段斜隔,左腔为子宫内膜样腺癌(II级,IA期)。未给予辅助治疗,患者术后2年康复。
临床医生应意识到,对于出现持续性子宫异常出血但子宫内膜活检阴性或子宫内膜活检手术失败的患者,可能存在子宫恶性肿瘤与子宫异常并存的情况。在这种情况下,磁共振成像在畸形和恶性肿瘤的诊断中具有重要作用,应进行剖腹探查以避免延误癌症的诊断和治疗。