Concurrent ependymal and ganglionic differentiation in a subset of supratentorial neuroepithelial tumors with EWSR1-PLAGL1 rearrangement
Neuroepithelial tumors with fusion of PLAGL1 or amplification of PLAGL1/PLAGL2 have recently been described often with ependymoma-like or embryonal histology respectively. To further evaluate emerging entities with PLAG-family genetic alterations, the histologic, molecular, clinical, and imaging features are described for 8 clinical cases encountered at St. Jude (EWSR1-PLAGL1 fusion n = 6; PLAGL1 amplification n = 1; PLAGL2 amplification n = 1). A histologic feature observed on initial resection in a subset (4/6) of supratentorial neuroepithelial tumors with EWSR1-PLAGL1 rearrangement was the presence of concurrent ependymal and ganglionic differentiation. This ranged from prominent clusters of ganglion cells within ependymoma/subependymoma-like areas, to interspersed ganglion cells of low to moderate frequency among otherwise ependymal-like histology, or focal areas with a ganglion cell component. When present, the combination of ependymal-like and ganglionic features within a supratentorial neuroepithelial tumor may raise consideration for an EWSR1-PLAGL1 fusion, and prompt initiation of appropriate molecular testing such as RNA sequencing and methylation profiling. One of the EWSR1-PLAGL1 fusion cases showed subclonal INI1 loss in a region containing small clusters of rhabdoid/embryonal cells, and developed a prominent ganglion cell component on recurrence. As such, EWSR1-PLAGL1 neuroepithelial tumors are a tumor type in which acquired inactivation of SMARCB1 and development of AT/RT features may occur and lead to clinical progression. In contrast, the PLAGL2 and PLAGL1 amplified cases showed either embryonal histology or contained an embryonal component with a significant degree of desmin staining, which could also serve to raise consideration for a PLAG entity when present. Continued compilation of associated clinical data and histopathologic findings will be critical for understanding emerging entities with PLAG-family genetic alterations.
Authors
- Sonika M Dahiya (ORCID: https://orcid.org/0000-0002-5585-0964)
- Murat Gökden (ORCID: https://orcid.org/0000-0001-5275-1672)
- Julieann C. Lee (ORCID: https://orcid.org/0000-0003-0138-4862)
- Daniel C. Moreira (ORCID: https://orcid.org/0000-0003-4082-156X)
- Kaleigh F. Roberts (ORCID: https://orcid.org/0000-0001-6483-9153)
- Kelsey C. Bertrand (ORCID: https://orcid.org/0000-0001-6382-5411)
- Asim K. Bag (ORCID: https://orcid.org/0000-0001-6164-5863)
- Alex Breuer
- Brent A. Orr (ORCID: https://orcid.org/0000-0003-0997-4728)
- Nicholas Willard (ORCID: https://orcid.org/0000-0003-4912-201X)
- Jenna L. Bodmer (ORCID: https://orcid.org/0000-0003-3110-6679)
- Trisha Larkin (ORCID: https://orcid.org/0000-0001-5701-898X)
- Giles W Robinson (ORCID: https://orcid.org/0000-0001-7441-9486)
- Selene C. Koo (ORCID: https://orcid.org/0000-0001-8459-2469)
- Larissa V. Furtado (ORCID: https://orcid.org/0000-0001-7784-9502)
- David W. Ellison (ORCID: https://orcid.org/0000-0003-1239-7757)
- Mohammad K. Eldomery (ORCID: https://orcid.org/0009-0005-5699-6008)
- Bette K. Kleinschmidt‐DeMasters (ORCID: https://orcid.org/0000-0002-4471-1678)
- Gary J. Rose (ORCID: https://orcid.org/0000-0003-1376-6737)
- Rick Sances
- Pat Stow
- Jun Qin Mo
Institutions
- St. Jude Children's Research Hospital (US)
- Washington University in St. Louis (US)
- Rady Children's Hospital-San Diego (US)
- St. Joseph's Hospital (US)
- East Tennessee Children's Hospital (US)
- University of Arkansas for Medical Sciences (US)
- University of Colorado Denver (US)
Publication Details
- Journal
- Acta Neuropathologica Communications
- Published
- 2024-09-03
- DOI
- https://doi.org/10.1186/s40478-024-01809-9
- Citations
- 2
- Primary Topic
- Chromatin Remodeling and Cancer
- Type
- article
- Field-Weighted Citation Impact
- 0.47
Funders
- St. Jude Children's Research Hospital