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1例罕见的低级别子宫内膜间质肉瘤侵犯陈旧性平滑肌瘤病例

A Rare Case of Low-Grade Endometrial Stromal Sarcoma Invading an Old Leiomyoma.

作者信息

Inoue Kayo, Kuroshima Mizuho, Murata Yuka, Morita Hiroki

机构信息

Obstetrics and Gynecology, Konan Medical Center, Kobe, JPN.

Obstetrics and Gynecology, Kobe Children's Hospital, Kobe, JPN.

出版信息

Cureus. 2024 Nov 9;16(11):e73329. doi: 10.7759/cureus.73329. eCollection 2024 Nov.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f4ee/11626990/35c7a85aacec/cureus-0016-00000073329-i01.jpg

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