Department of Pathology, Guiqian International General Hospital, Guiyang, Guizhou Province, China.
Department of Radiology, Guiqian International General Hospital, Guiyang, Guizhou Province, China.
Sci Prog. 2024 Oct-Dec;107(4):368504241296291. doi: 10.1177/00368504241296291.
Uterine adenosarcoma coexisting with endometrial carcinoma is a very rare disease. Herein, we reported the case of uterine adenosarcoma coexisting with endometrioid endometrial carcinoma. Transvaginal ultrasound, computed tomography, and magnetic resonance imaging examinations all indicated a space-occupying lesion in the uterine cavity, and initially was considered endometrial carcinoma. Subsequently, total hysterectomy combined with bilateral salpingo-oophorectomy, pelvic lymphadenectomy, and para-aortic lymphadenectomy were performed. The coexistence of uterine adenosarcoma and endometrioid endometrial carcinoma was histologically confirmed postoperatively. The patient recovered well after surgery and was discharged on postoperative day 7. At a follow-up examination 10 months after surgery, we found no evidence of discomforting symptoms and recurrence or metastasis. Since the coexistence of uterine adenosarcoma and endometrial carcinoma is rare, it is easy to be overlooked the presence of uterine adenosarcoma on imaging or morphology, and thus be misdiagnosed as a more common disease, namely endometrial carcinoma. Observing the cystic structure within the lesion on magnetic resonance imaging is helpful for the diagnosis of uterine adenosarcoma. This article summarizes the imaging characteristics, clinicopathological features, molecular correlation, treatment, and prognosis of the disease.
同时患有子宫腺肉瘤和子宫内膜癌是一种非常罕见的疾病。本文报道了一例同时患有子宫腺肉瘤和子宫内膜样腺癌的病例。经阴道超声、计算机断层扫描和磁共振成像检查均提示宫腔占位性病变,最初被认为是子宫内膜癌。随后,行全子宫切除术加双侧附件切除术、盆腔淋巴结切除术和腹主动脉旁淋巴结切除术。术后组织病理学检查证实同时患有子宫腺肉瘤和子宫内膜样腺癌。患者术后恢复良好,术后第 7 天出院。术后 10 个月随访时,患者无不适症状,无复发或转移。由于子宫腺肉瘤和子宫内膜癌同时存在的情况较为罕见,因此在影像学或形态学上容易忽略子宫腺肉瘤的存在,从而误诊为更为常见的疾病,即子宫内膜癌。磁共振成像上观察到病变内的囊性结构有助于子宫腺肉瘤的诊断。本文总结了该病的影像学特征、临床病理特征、分子相关性、治疗和预后。