Clinical and molecular features of primary spinal epidural lymphomas

Lymphomas confined to the spinal epidural space at initial diagnosis are rare and referred to as primary spinal epidural lymphoma (PSEL). This study presents clinical, histopathological, and molecular insights from 13 PSEL cases, including follicular lymphoma (PSEL-FL, N = 4), extranodal marginal zone lymphoma (PSEL-MZL, N = 3), diffuse large B-cell lymphoma (PSEL-DLBCL, N = 5), and Burkitt lymphoma (PSEL-BL, N = 1). Despite localized presentation at initial diagnosis, PSEL with aggressive histologies demonstrated remarkably unfavorable outcomes, contrasting the highly indolent clinical course observed in indolent PSEL, particularly PSEL-FL. Molecular analysis showed similarities to nodal counterparts and separation by entity. Comparison of PSEL-FL and classic FL revealed activated tumor microenvironment-associated pathways, potentially supporting extranodal lymphoma growth in this rarely affected spinal epidural site.

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Publication Details

Journal
Annals of Hematology
Published
2025-09-25
DOI
https://doi.org/10.1007/s00277-025-06554-0
Primary Topic
Lymphoma Diagnosis and Treatment
Type
article
Field-Weighted Citation Impact
0.00

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article

Clinical and molecular features of primary spinal epidural lymphomas

Verena Passerini, Martina Rudelius, Michael Heide, Michael von Bergwelt‐Baildon et al.
Annals of Hematology
Lymphoma Diagnosis and Treatment
article

Clinical and molecular features of primary spinal epidural lymphomas

Verena Passerini, Martina Rudelius, Michael Heide, Michael von Bergwelt‐Baildon, Stefan Zausinger, Louisa von Baumgarten, Sophia Stoecklein, Philipp Karschnia, Christian Schichor, Oliver Weigert, Veit M. Stoecklein, Niklas Thon, Louisa Adolph, Jörg C. Tonn
article en

Abstract

Lymphomas confined to the spinal epidural space at initial diagnosis are rare and referred to as primary spinal epidural lymphoma (PSEL). This study presents clinical, histopathological, and molecular insights from 13 PSEL cases, including follicular lymphoma (PSEL-FL, N = 4), extranodal marginal zone lymphoma (PSEL-MZL, N = 3), diffuse large B-cell lymphoma (PSEL-DLBCL, N = 5), and Burkitt lymphoma (PSEL-BL, N = 1). Despite localized presentation at initial diagnosis, PSEL with aggressive histologies demonstrated remarkably unfavorable outcomes, contrasting the highly indolent clinical course observed in indolent PSEL, particularly PSEL-FL. Molecular analysis showed similarities to nodal counterparts and separation by entity. Comparison of PSEL-FL and classic FL revealed activated tumor microenvironment-associated pathways, potentially supporting extranodal lymphoma growth in this rarely affected spinal epidural site.

Annals of HematologyVol. 104(10)
German Cancer Research Center (DE), Friedrich-Alexander-Universität Erlangen-Nürnberg (DE), Heidelberg University (DE), Ludwig-Maximilians-Universität München (DE)
Wilhelm Sander-Stiftung, Deutsche Forschungsgemeinschaft, Else Kröner-Fresenius-Stiftung
Openalex Percentile: Top 63%
Lymphoma Diagnosis and Treatment
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