Devalla Anusha, Mangla Mishu, Ramavath Krishna, Prabhala Shailaja, Kumar Naina, Jarathi Aparna
Department of Obstetrics and Gynecology, All India Institute of Medical Sciences, Bibinagar, Hyderabad 508126, India.
Department of General Surgery, All India Institute of Medical Sciences, Bibinagar, Hyderabad 508126, India.
Oncoscience. 2025 Feb 10;12:21-25. doi: 10.18632/oncoscience.615. eCollection 2025.
Postmenopausal bleeding (PMB) with a diffusely enlarged uterus necessitates Magnetic Resonance Imaging (MRI) to reach an accurate diagnosis. Adenomyosis, especially extensive glandular variant, is an extremely rare cause reported in a postmenopausal woman. We present a challenging case of an 81-year-old woman with PMB where preoperative MRI suggested possible invasive endometrial neoplasm. However, final histopathological evidence of the hysterectomy specimen suggested Adenomyosis with extensive glandular proliferation. The patient was a multiparous lady with controlled diabetes and hypertension (controlled on medications) and a Body Mass Index of 36 kg/m. Bimanual examination suggested a diffusely enlarged uterus corresponding to 8-10 weeks gestation. Transvaginal ultrasound (TVUS) and Contrast Enhanced (CE) MRI were performed that reported multiple cystic areas with myometrial thinning at the fundal region- suspected infiltrating endometrial neoplasm. A hysteroscopic guided endometrial biopsy was suggestive of endometrial hyperplasia. In view of concerning MRI findings, a total abdominal hysterectomy and bilateral Salpingo-oophorectomy was performed. Histopathological examination revealed Adenomyosis with extensive glandular proliferation co-existing with endometrial hyperplasia and no atypia. This case highlights an important variant of Adenomyosis that potentially mimics an invasive uterine neoplasm. There is a dearth of uniform reporting standards for Adenomyosis and rarity of this condition in postmenopausal woman posing a significant preoperative diagnostic challenge.
绝经后出血(PMB)伴有子宫弥漫性增大时,需要进行磁共振成像(MRI)以做出准确诊断。子宫腺肌病,尤其是广泛的腺性变异型,是绝经后女性中报道的极为罕见的病因。我们报告一例具有挑战性的病例,一名81岁患有PMB的女性,术前MRI提示可能为侵袭性子宫内膜肿瘤。然而,子宫切除标本的最终组织病理学证据显示为伴有广泛腺体增生的子宫腺肌病。患者为经产妇,患有糖尿病和高血压(药物控制良好),体重指数为36kg/m。双合诊检查提示子宫弥漫性增大,相当于妊娠8 - 10周。进行了经阴道超声(TVUS)和对比增强(CE)MRI检查,报告在宫底区域有多个囊性区域伴肌层变薄,怀疑为浸润性子宫内膜肿瘤。宫腔镜引导下的子宫内膜活检提示子宫内膜增生。鉴于MRI检查结果令人担忧,遂进行了全腹子宫切除术和双侧输卵管卵巢切除术。组织病理学检查显示,子宫腺肌病伴有广泛腺体增生,同时存在子宫内膜增生且无异型性。该病例突出了子宫腺肌病的一种重要变异型,其可能酷似侵袭性子宫肿瘤。目前缺乏关于子宫腺肌病统一的报告标准,且这种情况在绝经后女性中罕见,给术前诊断带来了重大挑战。