Southwest Medical University, Luzhou, 646099, China.
University of Electronic Science and Technology of China, Chengdu, 610054, China.
BMC Womens Health. 2024 Aug 2;24(1):440. doi: 10.1186/s12905-024-03170-4.
Carcinomatous changes from the ectopic endometrial glands in endometriosis have been reported in many studies, but malignant transformation from uterine adenomyosis/adenomyoma is rare. And clear cell-like adenocarcinoma represents a seldom-encountered malignant pathological variant of ectopic endometrium.
This case report presents a case of a 44-year-old nulliparous woman begun with abdominal pain and intestinal obstruction. Past medical history showed laparoscopic ovarian endometriotic cyst excision. Ultrasound indicated adenomyoma and a parametrial hypoechoic nodule with abundant blood flow signals and unclear boundaries. Deep invasive endometriosis was considered preoperatively. The patient underwent laparoscopic subtotal hysterectomy and bilateral adnexa resection. Chocolate cyst-like lesion was observed in the parametral lesion. Postoperative pathological examinations suggested endometrioid adenocarcinoma arising from eutopic endometrium and adenomyoma. Ectopic endometrium in the myometrium combined with atypical hyperplasia and formation of endometrioid adenocarcinoma. Left parametrial lesions suggested poorly differentiated endometrioid adenocarcinoma combined with clear cell carcinoma. CD10 + endometrial stromal cells were observed surrounding tumor cell masses. Combined with surgical founding and pathological characters of the left parametrial adenocarcinoma, the parametrial lesions were more likely to be carcinomatous changes of the original deep endometriosis.The patient underwent subsequent transabdominal tumor cell reduction surgery and chemotherapy.
We herein present a rare case of combined endometrioid adenocarcinoma arising from uterine adenomyosis and clear cell carcinoma arising from parametrial deep endometriosis that may help inspire additional studies in the future. The patient underwent robot-assisted laparoscopic subtotal hysterectomy, bilateral adnexa resection, deep endometriosis lesion resection and bilateral ureteral stent placement. Following surgery, a chemotherapy regimen of Taxol and Carboplatin was administered.
在许多研究中都报道了子宫内膜异位症的异位子宫内膜腺体发生癌变,但子宫腺肌病/腺肌瘤恶变则很少见。透明细胞样腺癌是异位子宫内膜罕见的恶性病理变异型。
本病例报告介绍了一位 44 岁未育的女性,最初出现腹痛和肠梗阻。既往病史显示腹腔镜卵巢子宫内膜异位囊肿切除术。超声提示腺肌瘤和子宫旁低回声结节,血流信号丰富,边界不清。术前考虑深部浸润性子宫内膜异位症。患者接受了腹腔镜次全子宫切除术和双侧附件切除术。在子宫旁病变中观察到巧克力囊肿样病变。术后病理检查提示来源于子宫内膜的子宫内膜样腺癌和腺肌瘤。子宫肌层异位子宫内膜伴非典型增生和子宫内膜样腺癌形成。左侧子宫旁病变提示低分化子宫内膜样腺癌合并透明细胞癌。可见 CD10+子宫内膜间质细胞围绕肿瘤细胞团。结合左侧子宫旁腺癌的手术发现和病理特征,子宫旁病变更可能是深部子宫内膜异位症的癌性改变。患者随后接受了经腹肿瘤细胞减灭术和化疗。
本文报道了一例罕见的子宫腺肌病合并子宫内膜样腺癌和源自子宫旁深部子宫内膜异位症的透明细胞癌的病例,可能有助于未来的进一步研究。患者接受了机器人辅助腹腔镜次全子宫切除术、双侧附件切除术、深部子宫内膜异位症病灶切除术和双侧输尿管支架置入术。术后给予紫杉醇联合卡铂化疗方案。