Habek Dubravko, Dmitrovic Branko, Popovic Zoran, Karsa Matija, Blazicvic Valerija, Rupcic Branko, Vlahovic Mirna Erman, Marjanovic Ksenija
Department of Obstetrics and Gynecology, School of Medicine, Zagreb University, Sveti Duh Hospital Zagreb, Zagreb, Croatia.
J Obstet Gynaecol Res. 2006 Apr;32(2):212-5. doi: 10.1111/j.1447-0756.2006.00379.x.
We present an extremely rare case of a successfully operated giant (6700 g) paraovarian myxoma and uterus myomatosus in a 49-year-old woman. Preoperative examination (biochemical investigations, ultrasound and computed tomography scan) and perioperative findings did not identify a malignant tumor so that total abdominal hysterectomy/bilateral salpingo-oophorectomy and tumorectomy was chosen to treat the patient. Histologically, the tumor was clearly differentiated from the surrounding tissue. In solid regions there were spindle-shaped cells arranged in sheaves and within the profuse, well-vascularized myxomatous stroma there were star-shaped cells. Immunohistochemical analysis showed that tumor cells were positive to vimentin and smooth muscle actin. Electron microscopic analysis showed that tumor cells had ultrastructural characteristics that corresponded to cells in fibroma and thecoma in a profuse intercellular matrix, which confirmed the result of light microscopy.
我们报告了一例极为罕见的病例,一名49岁女性成功接受了手术切除巨大(6700克)的卵巢旁黏液瘤和子宫肌瘤。术前检查(生化检查、超声和计算机断层扫描)及围手术期检查均未发现恶性肿瘤,因此选择行全腹子宫切除术/双侧输卵管卵巢切除术及肿瘤切除术来治疗该患者。组织学检查显示,肿瘤与周围组织有明显差异。在实性区域有呈束状排列的梭形细胞,在丰富且血管化良好的黏液瘤性间质内有星形细胞。免疫组织化学分析显示肿瘤细胞波形蛋白和平滑肌肌动蛋白呈阳性。电子显微镜分析显示肿瘤细胞具有超微结构特征,在丰富的细胞间基质中与纤维瘤和卵泡膜瘤细胞相对应,这证实了光学显微镜检查的结果。