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具有脂肪细胞分化的女性生殖道恶性平滑肌肿瘤:6 例脂肪平滑肌肉瘤的形态学、免疫组织化学、MDM2 荧光原位杂交和分子遗传学研究。

Malignant female genital tract smooth muscle tumors with adipocytic differentiation: A morphologic, immunohistochemical, MDM2 fluorescence in situ hybridization and molecular genetic study of 6 lipoleiomyosarcomas.

机构信息

Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.

Department of Pathology, Charles University, Faculty of Medicine in Pilsen, Pilsen, Czech Republic; Bioptical Laboratory, Ltd., Pilsen, Czech Republic.

出版信息

Hum Pathol. 2024 Jan;143:24-32. doi: 10.1016/j.humpath.2023.11.008. Epub 2023 Nov 23.

Abstract

Leiomyosarcoma with adipocytic differentiation or lipoleiomyosarcoma is an uncommon sarcoma of the female genital tract with only a few individual reports in the literature. We therefore performed a morphologic, immunohistochemical, MDM2 gene amplification and RNA and DNA sequencing analysis of a series of gynecologic lipoleiomyosarcoma to better define the clinicopathologic spectrum. Six tumors from 6 patients were identified and classified as spindled lipoleiomyosarcoma (n = 2), mixed spindled and myxoid lipoleiomyosarcoma (n = 1), epithelioid lipoleiomyosarcoma with focal myxoid features (n = 1) and mixed spindled and epithelioid lipoleiomyosarcoma (n = 2). Patient age ranged from 41 to 64 years (mean: 49; median: 50). Primary location included uterine corpus (3), uterine corpus/cervix (2) and broad ligament (1). Tumor size ranged from 4.5 to 22 cm (mean: 11.2; median: 9.8). Four patients had metastasis at presentation or subsequently developed recurrent or distant disease. Patient status was known for 5: 2 dead of disease, 2 alive with disease and 1 alive without evidence of disease. Immunohistochemical expression of smooth muscle markers, ER, PR and WT-1 showed patterns similar to non-adipocytic gynecologic leiomyosarcomas. MDM2 amplification fluorescence in situ hybridization performed on 2 tumors was negative in 1 and equivocal in 1. Sequencing studies performed on 3 tumors found TP53 mutations in 3, with 1 tumor also having an ATRX alteration. No gene fusions were identified. Although lipoleiomyosarcomas have a diverse morphologic spectrum, our findings suggest the smooth muscle component shares morphologic and immunohistochemical features with female genital tract non-adipocytic leiomyosarcomas. Lipoleiomyosarcomas also have genetic alterations associated with non-adipocytic gynecologic leiomyosarcomas.

摘要

具有脂肪细胞分化的平滑肌肉瘤或脂肪平滑肌肉瘤是一种罕见的女性生殖道肉瘤,文献中仅有少数个别报道。因此,我们对一系列妇科脂肪平滑肌肉瘤进行了形态学、免疫组织化学、MDM2 基因扩增以及 RNA 和 DNA 测序分析,以更好地定义其临床病理谱。从 6 名患者中确定了 6 个肿瘤,并将其分类为梭形脂肪平滑肌肉瘤(n=2)、梭形和黏液样混合脂肪平滑肌肉瘤(n=1)、局灶黏液样特征的上皮样脂肪平滑肌肉瘤(n=1)和梭形和上皮样混合脂肪平滑肌肉瘤(n=2)。患者年龄为 41 岁至 64 岁(平均:49 岁;中位数:50 岁)。原发部位包括子宫体(3 例)、子宫体/宫颈(2 例)和阔韧带(1 例)。肿瘤大小为 4.5 厘米至 22 厘米(平均:11.2 厘米;中位数:9.8 厘米)。4 名患者在就诊时出现转移,或随后出现复发性或远处疾病。已知 5 名患者的病情:2 例死亡,2 例存活伴疾病,1 例存活且无疾病证据。平滑肌标志物、ER、PR 和 WT-1 的免疫组织化学表达模式与非脂肪性妇科平滑肌肉瘤相似。对 2 个肿瘤进行的 MDM2 扩增荧光原位杂交在 1 个肿瘤中为阴性,在 1 个肿瘤中为不确定。对 3 个肿瘤进行的测序研究发现 3 个肿瘤均存在 TP53 突变,其中 1 个肿瘤还存在 ATRX 改变。未发现基因融合。尽管脂肪平滑肌肉瘤具有多样化的形态谱,但我们的研究结果表明,平滑肌成分具有与女性生殖道非脂肪性平滑肌肉瘤相似的形态和免疫组织化学特征。脂肪平滑肌肉瘤也存在与非脂肪性妇科平滑肌肉瘤相关的遗传改变。

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