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伴有 CCND1 基因重排的组织细胞肉瘤与套细胞淋巴瘤克隆相关且发生转分化。

Histiocytic Sarcoma With CCND1 Gene Rearrangement Clonally Related and Transdifferentiated From Mantle Cell Lymphoma.

机构信息

Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA.

Department of Pathology, University of Louisville School of Medicine, Louisville, KY, USA.

出版信息

Am J Clin Pathol. 2022 Oct 6;158(4):449-455. doi: 10.1093/ajcp/aqac087.

Abstract

OBJECTIVES

Histiocytic neoplasms demonstrate shared gene translocations and clonal immunoglobulin gene rearrangements in cases of associated B-cell lymphomas. However, the evolution of these related disease processes remains largely uncertain, especially in the setting of a prior mantle cell lymphoma.

METHODS

We describe a unique case of a histiocytic sarcoma that transdifferentiated from blastoid mantle cell lymphoma after extensive therapy. Cytogenic and molecular studies were performed and provided evidence for clonal progression.

RESULTS

We present the first reported case of a patient with blastoid mantle cell lymphoma harboring a CCND1 rearrangement that progressed despite multiple therapeutic regimens and ultimately transdifferentiated into histiocytic sarcoma. The histiocytic sarcoma demonstrated a CCND1 rearrangement and targeted next-generation sequencing showed a pathogenic variant in NRAS, a gene involved in the RAS/MAPK pathway, known to play a role in the pathogenesis of histiocytic sarcomas. TP53, NOTCH2, CREBBP, and NFKBIE variants were also identified, which are often seen in B-cell lymphomas, while rarely described in histiocytic sarcoma.

CONCLUSIONS

To our knowledge, this is the first report to provide evidence for clonal evolution of histiocytic sarcoma from blastoid mantle cell lymphoma based on cytogenic and molecular findings. The patient's protracted therapeutic course may have acted as an evolutionary driver promoting this transdifferentiation process.

摘要

目的

组织细胞肿瘤在伴有 B 细胞淋巴瘤的病例中表现出共享的基因易位和克隆免疫球蛋白基因重排。然而,这些相关疾病过程的演变在很大程度上仍然不确定,尤其是在先前存在套细胞淋巴瘤的情况下。

方法

我们描述了一例独特的组织细胞肉瘤病例,该病例在广泛治疗后从原始母细胞淋巴瘤的母细胞样淋巴瘤转化而来。进行了细胞遗传学和分子研究,并提供了克隆进展的证据。

结果

我们提出了首例报告的患者,其母细胞样套细胞淋巴瘤存在 CCND1 易位,尽管经过多种治疗方案,但仍进展并最终转化为组织细胞肉瘤。组织细胞肉瘤显示 CCND1 易位,靶向下一代测序显示 RAS/MAPK 通路中参与组织细胞肉瘤发病机制的基因 NRAS 存在致病性变异。还鉴定了 TP53、NOTCH2、CREBBP 和 NFKBIE 变异体,这些变异体通常见于 B 细胞淋巴瘤,而在组织细胞肉瘤中很少描述。

结论

据我们所知,这是第一个基于细胞遗传学和分子发现提供组织细胞肉瘤从母细胞样套细胞淋巴瘤克隆进化证据的报告。患者的长期治疗过程可能是促进这种转化过程的进化驱动因素。

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