Inoue Kayo, Kuroshima Mizuho, Murata Yuka, Morita Hiroki
Obstetrics and Gynecology, Konan Medical Center, Kobe, JPN.
Obstetrics and Gynecology, Kobe Children's Hospital, Kobe, JPN.
Cureus. 2024 Nov 9;16(11):e73329. doi: 10.7759/cureus.73329. eCollection 2024 Nov.
We present the first case of low-grade endometrial stromal sarcoma (ESS) invading a leiomyoma, which was difficult to diagnose preoperatively. A 49-year-old multiparous woman was referred to our institution due to the enlargement of an old leiomyoma after menopause. Transvaginal ultrasonography revealed a 40-mm lesion in the myometrium of the uterine body with calcification and edema. Color Doppler imaging showed blood flow along the margins of the mass. Pelvic contrast-enhanced magnetic resonance imaging (MRI) revealed a 39-mm mass in the uterine body, predominantly having a low intensity on T2-weighted images, suggesting leiomyoma containing a cystic lesion with a small solid component. This solid component appeared to have a high intensity on T2-weighted images, high intensity on diffusion-weighted images, low value on apparent diffusion coefficient (ADC) map images, and contrast effect. F-fluoro-deoxyglucose positron emission tomography (FDG-PET)-computed tomography (CT) showed a non-significant FDG uptake in the cyst's solid component. Based on a preoperative diagnosis of cystic or myxoid degeneration of leiomyoma, laparoscopic total hysterectomy and bilateral salpingo-oophorectomy were performed. The uterus was retrieved vaginally without morcellation. Macroscopic examination of the hysterectomy specimens revealed a 55-mm white solid tumor with scattered yellow nodules. Histopathological analysis identified spindle-shaped smooth muscle cells with non-atypical nuclei, confirming a leiomyoma. However, the tumor's nodules contained slightly atypical cells with round nuclei, resembling endometrial stromal cells interspersed with small blood vessels. Immunohistochemical staining showed the nodules were negative for alpha-smooth muscle actin and positive for CD-10, estrogen receptor, and progesterone receptor. These nodules invaded the leiomyoma along vascular vessels. The final diagnosis was leiomyoma coexisting with low-grade ESS, classified as International Federation of Gynecology and Obstetrics (FIGO) stage IB. The patient received no further treatment and remains disease-free after 45 months.
我们报告首例低级别子宫内膜间质肉瘤(ESS)侵犯平滑肌瘤的病例,该病例术前难以诊断。一名49岁经产妇因绝经后旧有平滑肌瘤增大而转诊至我院。经阴道超声检查发现子宫体肌层有一个40毫米的病灶,伴有钙化和水肿。彩色多普勒成像显示肿块边缘有血流。盆腔增强磁共振成像(MRI)显示子宫体有一个39毫米的肿块,在T2加权图像上主要呈低信号,提示为含有囊性病变及小实性成分的平滑肌瘤。该实性成分在T2加权图像上呈高信号,在扩散加权图像上呈高信号,在表观扩散系数(ADC)图图像上呈低值,并具有强化效应。F-氟脱氧葡萄糖正电子发射断层扫描(FDG-PET)计算机断层扫描(CT)显示囊肿实性成分的FDG摄取不显著。基于术前平滑肌瘤囊性或黏液样变性的诊断,实施了腹腔镜全子宫切除术和双侧输卵管卵巢切除术。经阴道取出子宫,未进行粉碎术。子宫切除标本的宏观检查显示一个55毫米的白色实性肿瘤,伴有散在的黄色结节。组织病理学分析发现梭形平滑肌细胞,核无异型性,证实为平滑肌瘤。然而,肿瘤结节含有核稍异型的圆形细胞,类似子宫内膜间质细胞,其间有小血管。免疫组化染色显示结节α-平滑肌肌动蛋白阴性,CD-10、雌激素受体和孕激素受体阳性。这些结节沿血管侵犯平滑肌瘤。最终诊断为平滑肌瘤合并低级别ESS,分类为国际妇产科联盟(FIGO)IB期。患者未接受进一步治疗,45个月后仍无疾病。