具有侵袭性的小儿原始圆形细胞瘤与 MN1::ZNF341 融合:神经母细胞瘤的模拟体

IF 2.4 3区 医学 Q2 HEMATOLOGY
Serena Y Tan, Mark G Evans, Raya Saab, Ankur Gupta, Jack Reid, Tuan Dao, Elyssa Rubin, Anthony Crymes, Kapitolina Semenova, Hiroyuki Shimada, Chad Livasy, Ali Nael
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引用次数: 0

摘要

神经母细胞瘤是幼儿最常见的肿瘤之一,起源于肾上腺髓质或脊髓交感神经节旁。我们描述了三例小于 1.5 岁的原始圆形细胞瘤患者,其临床和病理表现与神经母细胞瘤极为相似。然而,与神经母细胞瘤不同的是,这些原始细胞瘤没有显示神经母细胞分化的特异性组织学或免疫表型证据,而且携带MN1::ZNF341融合。所有患者都在接受神经母细胞瘤治疗后病情恶化,最终死于疾病。这些模仿神经母细胞瘤的高侵袭性肿瘤似乎是一个新颖独特的实体,需要进一步鉴定。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Aggressive Pediatric Primitive Round Cell Tumors with MN1::ZNF341 Fusion: A Mimic of Neuroblastoma.

Neuroblastoma is one of the most common tumors in young children, arising from the adrenal medulla or paraspinal sympathetic ganglia. We describe primitive round cell tumors presenting in three patients less than 1.5 years old, with striking clinical and pathologic similarities to neuroblastoma. Unlike neuroblastoma, however, these primitive tumors did not show specific histologic or immunophenotypic evidence of neuroblastic differentiation, and harbored a MN1::ZNF341 fusion. All patients progressed through neuroblastoma therapy and ultimately died of disease. These highly aggressive tumors mimicking neuroblastoma appear to be a novel and distinctive entity in need of further characterization.

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来源期刊
Pediatric Blood & Cancer
Pediatric Blood & Cancer 医学-小儿科
CiteScore
4.90
自引率
9.40%
发文量
546
审稿时长
1.5 months
期刊介绍: Pediatric Blood & Cancer publishes the highest quality manuscripts describing basic and clinical investigations of blood disorders and malignant diseases of childhood including diagnosis, treatment, epidemiology, etiology, biology, and molecular and clinical genetics of these diseases as they affect children, adolescents, and young adults. Pediatric Blood & Cancer will also include studies on such treatment options as hematopoietic stem cell transplantation, immunology, and gene therapy.
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