伴有破骨细胞样巨细胞的子宫纵隔肉瘤:2例病例报告及文献综述。

IF 1.6 4区 医学 Q3 OBSTETRICS & GYNECOLOGY
Zhengshan Chen, Jianling Ji, Evan Yung, Sue Ellen Martin, Saloni Walia
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引用次数: 0

摘要

伴有破骨细胞样巨细胞(OLGCs)的骨髓肉瘤(LMS)是一种罕见病,迄今仅有18例报道。目前尚不清楚这些破骨细胞样巨细胞是LMS的反应性成分还是恶性成分。在此,我们描述了2例伴有OLGCs的LMS的临床、组织学和分子特征,并对文献进行了简要回顾。在我们的2例病例中,OLGCs以CD68为标记,Ki67增殖指数较低,免疫组化结果显示平滑肌标记物未呈弥漫阳性。通过下一代测序,一个病例发现了具有临床意义的TP53基因突变,据报道,相当一部分传统的LMS都存在这种突变。在该病例中,根据免疫组化结果,OLGCs与LMS相比表现出不同的分子改变。虽然我们没有发现伴有OLGCs的LMS有独特的免疫表型或分子特征,但这项研究为这一罕见病例提供了更多数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Uterine Leiomyosarcoma With Osteoclast-like Giant Cells: Report of 2 Cases and Review of Literature.

Leiomyosarcoma (LMS) with osteoclast-like giant cells (OLGCs) is a rare entity with only 18 reported cases thus far. It is not known whether these OLGCs are a reactive or malignant component of LMS. Herein we describe the clinical, histologic, and molecular characteristics of 2 cases of LMS with OLGCs and perform a brief literature review. In 2 of our cases, the OLGCs, marked with CD68, had a low proliferation index with Ki67 and did not show diffuse positivity for smooth muscle markers by immunohistochemistry. By next-generation sequencing, one case harbored a clinically significant TP53 mutation, which has been reported in a significant subset of conventional LMSs. In this case, based on immunohistochemistry, OLGCs showed different molecular alterations as compared with LMS. Although we did not show a distinct immunophenotype or molecular profile for LMS with OLGCs, this study provides additional data on this rare entity.

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来源期刊
CiteScore
3.90
自引率
12.50%
发文量
154
审稿时长
6-12 weeks
期刊介绍: International Journal of Gynecological Pathology is the official journal of the International Society of Gynecological Pathologists (ISGyP), and provides complete and timely coverage of advances in the understanding and management of gynecological disease. Emphasis is placed on investigations in the field of anatomic pathology. Articles devoted to experimental or animal pathology clearly relevant to an understanding of human disease are published, as are pathological and clinicopathological studies and individual case reports that offer new insights.
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