通过基因分析可将低级别中枢成纤维性骨肉瘤与其相似的结缔组织增生纤维瘤区分开来。

Clinical Sarcoma Research Pub Date : 2018-08-23 eCollection Date: 2018-01-01 DOI:10.1186/s13569-018-0104-z
Wangzhao Song, Eva van den Berg, Thomas C Kwee, Paul C Jutte, Anne-Marie Cleton-Jansen, Judith V M G Bovée, Albert J Suurmeijer
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引用次数: 8

摘要

背景:我们研究了2例罕见的纤维性骨肿瘤,即结缔组织增生纤维瘤(DF)和类似结缔组织增生纤维瘤(DF样LGCOS)的低级别中央骨肉瘤(LGCOS)。由于DF和DF样LGOS的临床表现、影像学特征和组织病理学有很大的重叠,本研究的目的是探讨细胞遗传学分析、分子病理学和免疫组织化学在鉴别这两种拟态物中的价值。病例介绍:在DF中观察到CTNNB (S45F)突变和核β -连环蛋白免疫染色。DF-LGCOS具有CDK4扩增,免疫组化显示CDK4核强表达。此外,DF-LGCOS的核型显示13号染色体长臂(q12q32)的间质性杂合缺失,与RB1肿瘤抑制基因的缺失有关。结论:核型分析和分子遗传学分析有助于结论性诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Low-grade central fibroblastic osteosarcoma may be differentiated from its mimicker desmoplastic fibroma by genetic analysis.

Background: We studied two cases of rare fibrous bone tumors, namely desmoplastic fibroma (DF) and low-grade central osteosarcoma (LGCOS) resembling desmoplastic fibroma (DF-like LGCOS). As the clinical presentation, imaging features and histopathology of DF and DF-like LGOS show much overlap, the objective of this study was to investigate the value of cytogenetic analysis, molecular pathology and immunohistochemistry in discrimination of these two mimickers.

Case presentation: A mutation in CTNNB (S45F) and nuclear beta-catenin immunostaining were observed in DF. DF-LGCOS had amplification of CDK4 and showed strong nuclear expression of CDK4 by IHC. Moreover, the karyotype of DF-LGCOS showed an interstitial heterozygous deletion of the long arm of chromosome 13 (q12q32), associated with loss of the RB1 tumor suppressor gene.

Conclusions: Karyotyping and molecular genetic analysis may contribute to a conclusive diagnosis.

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期刊介绍: Clinical Sarcoma Research considers for publication articles related to research on sarcomas, including both soft tissue and bone. The journal publishes original articles and review articles on the diagnosis and treatment of sarcomas along with new insights in sarcoma research, which may be of immediate or future interest for diagnosis and treatment. The journal also considers negative results, especially those from studies on new agents, as it is vital for the medical community to learn whether new agents have been proven effective or ineffective within subtypes of sarcomas. The journal also aims to offer a forum for active discussion on topics of major interest for the sarcoma community, which may be related to both research results and methodological topics.
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