Aggressive Pediatric Primitive Round Cell Tumors with <i>MN1</i>::<i>ZNF341</i> 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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Publication Details

Journal
Pediatric Blood & Cancer
Published
2024-11-06
DOI
https://doi.org/10.1002/pbc.31425
Citations
2
Primary Topic
Neuroblastoma Research and Treatments
Type
article
Field-Weighted Citation Impact
0.74
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article

Aggressive Pediatric Primitive Round Cell Tumors with MN1::ZNF341 Fusion: A Mimic of Neuroblastoma

Hiroyuki Shimada, Serena Y. Tan, Anthony Crymes, Chad Livasy et al.
2 citations
Pediatric Blood & Cancer
Neuroblastoma Research and Treatments
0.74
article

Aggressive Pediatric Primitive Round Cell Tumors with MN1::ZNF341 Fusion: A Mimic of Neuroblastoma

Hiroyuki Shimada, Serena Y. Tan, Anthony Crymes, Chad Livasy, Ali Nael, Kapitolina Semenova, Tuan Dao, Elyssa Rubin, Ankur Gupta, Raya Saab, Mark G. Evans, J. Reid
article en
2 citations

Abstract

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.

Pediatric Blood & CancerVol. 72(1)
University of Southern California (US), Children's Hospital of Orange County (US), University of California, Irvine Medical Center (US), Atrium Medical Cente (US), Caris Life Sciences (United States) (US), Stanford University (US)
Good health and well-being
Openalex Percentile: Top 26%
Neuroblastoma Research and Treatments
0.74
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