6个月大的bcor改变肉瘤:诊断挑战和形态学见解。

IF 0.7 4区 医学 Q4 PATHOLOGY
Fetal and Pediatric Pathology Pub Date : 2025-07-01 Epub Date: 2025-06-03 DOI:10.1080/15513815.2025.2512344
Shiv Shankar Verma, Lavleen Singh, Aditya Gupta
{"title":"6个月大的bcor改变肉瘤:诊断挑战和形态学见解。","authors":"Shiv Shankar Verma, Lavleen Singh, Aditya Gupta","doi":"10.1080/15513815.2025.2512344","DOIUrl":null,"url":null,"abstract":"<p><p>BCOR-altered sarcomas (BAS) are a subset of undifferentiated small round cell sarcomas characterized by alterations involving the BCOR gene. These tumors often pose diagnostic challenges due to their morphological overlap with other pediatric neoplasms. We report a case of BAS in an infant presenting with bilateral lower limb weakness. Imaging revealed a large multilobulated retroperitoneal mass. Histopathology showed prominent rhabdoid cells, alongside small round cells and spindle cells in a fascicular pattern. The tumor was positive for BCOR, Cyclin D1, TLE-1, BCL-6, and SATB2, while INI1 and BRG expression were retained. Fluoresence in situ hybridization, ruled out BCOR::CCNB3 fusion and NTRK 1/2/3 rearrangements. Based on the histopathological, immunophenotypic, and molecular profile, a diagnosis of BAS was established. The patient was started on a Ewing sarcoma chemotherapy regimen, showing a favourable response. This case highlights that BAS may rarely show a prominent rhabdoid feature and utility of ancillary diagnostic modalities.</p>","PeriodicalId":50452,"journal":{"name":"Fetal and Pediatric Pathology","volume":" ","pages":"333-338"},"PeriodicalIF":0.7000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"BCOR-Altered Sarcoma in a 6-Month-Old: Diagnostic Challenges and Morphological Insights.\",\"authors\":\"Shiv Shankar Verma, Lavleen Singh, Aditya Gupta\",\"doi\":\"10.1080/15513815.2025.2512344\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>BCOR-altered sarcomas (BAS) are a subset of undifferentiated small round cell sarcomas characterized by alterations involving the BCOR gene. These tumors often pose diagnostic challenges due to their morphological overlap with other pediatric neoplasms. We report a case of BAS in an infant presenting with bilateral lower limb weakness. Imaging revealed a large multilobulated retroperitoneal mass. Histopathology showed prominent rhabdoid cells, alongside small round cells and spindle cells in a fascicular pattern. The tumor was positive for BCOR, Cyclin D1, TLE-1, BCL-6, and SATB2, while INI1 and BRG expression were retained. Fluoresence in situ hybridization, ruled out BCOR::CCNB3 fusion and NTRK 1/2/3 rearrangements. Based on the histopathological, immunophenotypic, and molecular profile, a diagnosis of BAS was established. The patient was started on a Ewing sarcoma chemotherapy regimen, showing a favourable response. This case highlights that BAS may rarely show a prominent rhabdoid feature and utility of ancillary diagnostic modalities.</p>\",\"PeriodicalId\":50452,\"journal\":{\"name\":\"Fetal and Pediatric Pathology\",\"volume\":\" \",\"pages\":\"333-338\"},\"PeriodicalIF\":0.7000,\"publicationDate\":\"2025-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Fetal and Pediatric Pathology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1080/15513815.2025.2512344\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/6/3 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q4\",\"JCRName\":\"PATHOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Fetal and Pediatric Pathology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/15513815.2025.2512344","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/6/3 0:00:00","PubModel":"Epub","JCR":"Q4","JCRName":"PATHOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

BCOR改变肉瘤(BAS)是一种未分化的小圆细胞肉瘤,其特征是BCOR基因的改变。这些肿瘤由于其形态与其他儿科肿瘤重叠,常常构成诊断挑战。我们报告一例BAS在一个婴儿表现为双侧下肢无力。影像学显示腹膜后有一个大的多分叶状肿块。组织病理学显示突出的横纹肌样细胞,小圆形细胞和梭形细胞呈束状分布。BCOR、Cyclin D1、TLE-1、BCL-6、SATB2表达阳性,INI1、BRG表达不变。荧光原位杂交,排除BCOR::CCNB3融合和NTRK 1/2/3重排。根据组织病理学、免疫表型和分子特征,建立了BAS的诊断。患者开始接受尤因肉瘤化疗方案,显示出良好的反应。本病例强调BAS可能很少表现出突出的横纹肌特征和辅助诊断方式的实用性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
BCOR-Altered Sarcoma in a 6-Month-Old: Diagnostic Challenges and Morphological Insights.

BCOR-altered sarcomas (BAS) are a subset of undifferentiated small round cell sarcomas characterized by alterations involving the BCOR gene. These tumors often pose diagnostic challenges due to their morphological overlap with other pediatric neoplasms. We report a case of BAS in an infant presenting with bilateral lower limb weakness. Imaging revealed a large multilobulated retroperitoneal mass. Histopathology showed prominent rhabdoid cells, alongside small round cells and spindle cells in a fascicular pattern. The tumor was positive for BCOR, Cyclin D1, TLE-1, BCL-6, and SATB2, while INI1 and BRG expression were retained. Fluoresence in situ hybridization, ruled out BCOR::CCNB3 fusion and NTRK 1/2/3 rearrangements. Based on the histopathological, immunophenotypic, and molecular profile, a diagnosis of BAS was established. The patient was started on a Ewing sarcoma chemotherapy regimen, showing a favourable response. This case highlights that BAS may rarely show a prominent rhabdoid feature and utility of ancillary diagnostic modalities.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
3.00
自引率
0.00%
发文量
68
审稿时长
6-12 weeks
期刊介绍: Fetal and Pediatric Pathology is an established bimonthly international journal that publishes data on diseases of the developing embryo, newborns, children, and adolescents. The journal publishes original and review articles and reportable case reports. The expanded scope of the journal encompasses molecular basis of genetic disorders; molecular basis of diseases that lead to implantation failures; molecular basis of abnormal placentation; placentology and molecular basis of habitual abortion; intrauterine development and molecular basis of embryonic death; pathogenisis and etiologic factors involved in sudden infant death syndrome; the underlying molecular basis, and pathogenesis of diseases that lead to morbidity and mortality in newborns; prenatal, perinatal, and pediatric diseases and molecular basis of diseases of childhood including solid tumors and tumors of the hematopoietic system; and experimental and molecular pathology.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信