Bao Lingjie, Wang Ting, Xiao Yinping, Gu Shouxin, Zhou Xiaoyu, Zheng Yunxi, Chen Yun, Yi Xiaofang
Department of Gynecology, Obstetrics and Gynecology Hospital, Fudan University, Shanghai, China.
Department of Pathology, Obstetrics and Gynecology Hospital, Fudan University, Shanghai, China.
Heliyon. 2025 Jan 3;11(2):e41543. doi: 10.1016/j.heliyon.2024.e41543. eCollection 2025 Jan 30.
Pregnancy is a special time during which some benign hormonally-responsive lesions could grow and mimic malignancy on clinical evaluation and imaging. Though decidualization of ovarian endometrioma has been reported, little is known about decidualization of deep endometriosis. Here we report a case of decidualized bilateral ovarian endometriomas and rectouterine deep endometriosis mimicking as malignant lesions in the second-trimester of pregnancy.
A 26-year-old woman at 14 weeks of gestation presented to our hospital for the first time routine examination. Transvaginal ultrasound (TVS) showed bilateral adnexal masses of uneven echo with size 8.7 × 7.3 cm in the left ovary and size 5.5 × 4.8 cm in the right ovary, and another cystic mass with size 3.3 × 3.1 cm at rectouterine pouch. Serial nuclear magnetic resonance imaging (MRI) without contrast media for further evaluation indicated that these newly found pelvic masses were suspected to be ovarian endometrioid carcinoma with a metastasized lesion at rectouterine pouch. Serum CA125 was 56.7 U/L. HE-4 was 73.9 U/L. Considering that potential malignancy imaging had never been detected before pregnancy, multidisciplinary discussion (MDT) with doctors from obstetrics, gynecology, radiology and pathology department was organized at once. Conservative laparoscopic surgery was suggested to determine the pathology first. When removing the ovarian cysts and the lesion at rectouterine pouch, rich papillary nodules inside the capsule were exposed and looked like malignancy. Fortunately, frozen section revealed these lesions to be decidualized endometrioma. This patient recovered well and then went to the department of obstetrics for high-risk pregnancy supervision. Finally, the baby was delivered at 39 weeks by cesarean section because of fetal growth restriction (FGR).
Decidualization of endometriomas, especially deep endometriosis during pregnancy brings great challenge for clinical practice. A mature multidisciplinary team shows essential importance during treatment decisions. Early diagnosis of endometriosis before pregnancy help identify malignancy and reduce potential risks of maternal and fetal complications.
孕期是一段特殊时期,在此期间一些良性激素反应性病变可能生长,并在临床评估和影像学检查中表现出类似恶性肿瘤的特征。尽管已有卵巢子宫内膜异位囊肿蜕膜样变的报道,但对于深部子宫内膜异位症的蜕膜样变却知之甚少。在此,我们报告一例妊娠中期双侧卵巢子宫内膜异位囊肿及直肠子宫陷凹深部子宫内膜异位症蜕膜样变并酷似恶性病变的病例。
一名妊娠14周的26岁女性首次来我院进行常规检查。经阴道超声(TVS)显示双侧附件区有回声不均匀的包块,左侧卵巢包块大小为8.7×7.3cm,右侧卵巢包块大小为5.5×4.8cm,直肠子宫陷凹处还有一个大小为3.3×3.1cm的囊性包块。为进一步评估,连续进行了无造影剂的核磁共振成像(MRI)检查,结果提示这些新发现的盆腔包块疑似卵巢子宫内膜样癌并伴有直肠子宫陷凹处转移灶。血清CA125为56.7U/L,HE-4为73.9U/L。考虑到妊娠前从未检测到潜在的恶性影像学表现,当即组织了产科、妇科、放射科及病理科医生进行多学科讨论(MDT)。建议先进行保守性腹腔镜手术以确定病理。在切除卵巢囊肿及直肠子宫陷凹处病变时,囊内可见丰富的乳头状结节,看似恶性肿瘤。幸运的是,冰冻切片显示这些病变为蜕膜样变的子宫内膜异位囊肿。该患者恢复良好,随后前往产科进行高危妊娠监护。最终,因胎儿生长受限(FGR),患者于39周行剖宫产分娩。
子宫内膜异位囊肿的蜕膜样变,尤其是孕期深部子宫内膜异位症,给临床实践带来了巨大挑战。成熟的多学科团队在治疗决策过程中至关重要。妊娠前对子宫内膜异位症的早期诊断有助于识别恶性病变并降低母婴并发症的潜在风险。