PLAG1重排的子宫脂肪肉瘤1例,难以划分已建立的亚型

IF 1.6 4区 医学 Q3 OBSTETRICS & GYNECOLOGY
Junka Koyama, Kota Washimi, Akihiko Yoshida, Hiroyuki Shigeta, Chie Murata, Hiroyuki Hayashi
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引用次数: 0

摘要

在此,我们报告一例国际妇产科联合会IIIB期(pT3bNxM0)子宫脂肪肉瘤。虽然进行了强化肿瘤切除术,但患者在手术后53天死亡。切除的肿瘤表面呈淡黄色出血性梗死。组织学上,粘液样间质中可见脂肪细胞和成脂细胞。免疫组化检查显示,肿瘤弥漫性PLAG1(多形性腺瘤基因1)阳性,局灶性S100蛋白和CDK10阳性。肿瘤平滑肌肌动蛋白、desmin、MDM2、CDK4、ER、ALK、STAT6、NKX2.2、SS18、DDIT3、BCOR、pan-TRK均阴性。荧光原位杂交显示肿瘤存在PLAG1基因重排。然而,使用RNA测序分析进一步检查未能确定特定序列。由于肿瘤难以划分为脂肪肉瘤的四种亚型,目前的疾病可能是一种新型的子宫脂肪肉瘤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A case of uterine liposarcoma with PLAG1 rearrangement that was difficult to classify into established subtypes

Herein, we present a case of International Federation of Gynecology and Obstetrics stage IIIB (pT3bNxM0) uterine liposarcoma. Although intensive tumor resection was performed, the patient died 53 days after surgery. The resected surface of the tumor showed a yellowish hemorrhagic infarction. Histologically, adipocytes and lipoblasts were observed in the myxoid stroma. Immunohistochemical examination revealed that the tumor was diffusely positive for PLAG1 (pleomorphic adenoma gene 1) and focally positive for S100 protein and CDK10. The tumor was negative for smooth muscle actin, desmin, MDM2, CDK4, ER, ALK, STAT6, NKX2.2, SS18, DDIT3, BCOR, and pan-TRK. Fluorescence in situ hybridization showed that the tumor had a PLAG1 gene rearrangement. However, further examination using RNA sequencing analysis failed to identify specific sequences. As the tumor was difficult to classify into the four subtypes of liposarcoma, the current disease might be a new type of uterine liposarcoma.

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来源期刊
CiteScore
3.10
自引率
0.00%
发文量
376
审稿时长
3-6 weeks
期刊介绍: The Journal of Obstetrics and Gynaecology Research is the official Journal of the Asia and Oceania Federation of Obstetrics and Gynecology and of the Japan Society of Obstetrics and Gynecology, and aims to provide a medium for the publication of articles in the fields of obstetrics and gynecology. The Journal publishes original research articles, case reports, review articles and letters to the editor. The Journal will give publication priority to original research articles over case reports. Accepted papers become the exclusive licence of the Journal. Manuscripts are peer reviewed by at least two referees and/or Associate Editors expert in the field of the submitted paper.
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