Takeuchi K, Kitazawa S, Deguchi M, Maruo T
Department of Obstetrics and Gynecology, Kobe University Graduate School of Medicine, Japan.
Eur J Gynaecol Oncol. 2005;26(5):511-3.
A 83-year-old woman received bilateral salpingo-oophorectomy and hysterectomy due to a provisional diagnosis of ovarian cystic tumor. The tumor had a unilocular cystic cavity demonstrating serous cystadenoma and a solid mural nodule representing a biphasic pattern with mesenchymal and glandular components. The glandular elements were composed of benign serous cells, whereas the mesenchymal components consisted of an admixture of fibromatous stromal cells without atypia and sarcomatous overgrowth. The area of transition from a fibromatous component to sarcomatous overgrowth was identified. After a 2-year follow-up, there were no signs of tumor recurrence or systemic disease. To the authors' knowledge, this is the first reported case of adenofibrosarcoma originating from a mural nodule of ovarian serous cystadenoma.
一名83岁女性因初步诊断为卵巢囊性肿瘤接受了双侧输卵管卵巢切除术和子宫切除术。肿瘤有一个单房囊性腔,显示为浆液性囊腺瘤,还有一个实性壁结节,呈现出具有间叶和腺性成分的双相模式。腺性成分由良性浆液性细胞组成,而间叶成分则由无异型性的纤维瘤样基质细胞和肉瘤样过度生长混合而成。确定了从纤维瘤样成分到肉瘤样过度生长的过渡区域。经过2年随访,没有肿瘤复发或全身性疾病的迹象。据作者所知,这是首例源自卵巢浆液性囊腺瘤壁结节的腺纤维肉瘤报告病例。