Department of Gynecological Oncology, Kawasaki Medical School, Kurashiki, Japan.
Fukushima Medical Center for Children and Women, Fukushima Medical University, 1 Hikarigaoka, Fukushima City, Fukushima, 960-1295, Japan.
World J Surg Oncol. 2020 Dec 11;18(1):329. doi: 10.1186/s12957-020-02105-1.
Endometriosis can potentially lead to the development of a malignant tumor. Most malignant tumors arising from the endometriosis originate from the ovarian endometrioma, whereas those arising from extragonadal lesions are rare. We report a rare case of endometrioid carcinoma that developed from deep infiltrating endometriosis in the uterosacral ligament 6 years after treatment for atypical proliferative endometrioid tumor of the ovary in a 48-year-old woman.
Six years ago, the patient underwent laparoscopic bilateral salpingo-oophorectomy for her right ovarian tumor with atypical proliferative (borderline) endometrioid tumor accompanied by ovarian endometrioma. The solid tumor in the cul-de-sac was detected during follow-up using magnetic resonance imaging. Positron emission tomography/computed tomography revealed an abnormal accumulation of F-fluorodeoxyglucose at the tumor site. Thus, tumor recurrence with borderline malignancy was suspected. The patient underwent diagnostic laparoscopy followed by hysterectomy and partial omentectomy. Retroperitoneal pelvic lymphadenectomy and para-aortic lymphadenectomy were also performed. The cul-de-sac tumor at the left uterosacral ligament was microscopically diagnosed as invasive endometrioid carcinoma arising from deep infiltrating endometriosis. The final diagnosis was primary stage IIB peritoneal carcinoma. The patient received six courses of monthly paclitaxel and carboplatin as adjuvant chemotherapy. The patient showed no evidence of recurrence for 2 years after the treatments.
This study reports a rare case of metachronous endometriosis-related malignancy that developed 6 years after treatment for borderline ovarian tumor. If endometriosis lesions remain after bilateral salpingo-oophorectomy, the physician should keep the malignant nature of endometriosis in mind.
子宫内膜异位症可能导致恶性肿瘤的发展。大多数起源于卵巢子宫内膜异位症的恶性肿瘤来源于卵巢子宫内膜瘤,而起源于卵巢外病变的恶性肿瘤则较为罕见。我们报告了一例罕见的子宫内膜样癌病例,该病例发生于一名 48 岁女性,6 年前因卵巢非典型增生性子宫内膜样肿瘤接受双侧卵巢输卵管切除术及腹腔镜下腹膜切开术治疗,之后在宫骶韧带深部浸润性子宫内膜异位症中发展而来。
6 年前,该患者因右侧卵巢肿瘤行腹腔镜双侧卵巢输卵管切除术,肿瘤为伴卵巢子宫内膜瘤的非典型增生(交界性)子宫内膜样肿瘤。在随访中通过磁共振成像发现了阴道后穹窿的实性肿瘤。正电子发射断层扫描/计算机断层扫描显示肿瘤部位 F-氟脱氧葡萄糖异常积聚。因此,怀疑为交界性恶性肿瘤复发。患者行诊断性腹腔镜检查,随后行子宫切除术和部分网膜切除术。还进行了腹膜后盆腔淋巴结切除术和腹主动脉旁淋巴结切除术。左侧宫骶韧带阴道后穹窿肿瘤的显微镜检查诊断为深部浸润性子宫内膜异位症的侵袭性子宫内膜样癌。最终诊断为原发性 IIB 期腹膜癌。患者接受了 6 个疗程的每月紫杉醇联合卡铂辅助化疗。治疗后 2 年,患者未出现复发迹象。
本研究报告了一例罕见的子宫内膜异位症相关恶性肿瘤病例,该病例在治疗交界性卵巢肿瘤 6 年后发生。如果双侧卵巢输卵管切除术后仍存在子宫内膜异位症病变,医生应牢记子宫内膜异位症的恶性性质。