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May 11, 2026Journal of Clinical Laboratory Analysis0 citationsOpen Access

Isolated Pleural Effusion as Presentation of a Large B‐Cell Lymphoma: A Case Report and Diagnostic Considerations

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VMVan Vlierberghe MagalieDRDewaide RosinaMLMichaux Lucienne

Key Points

  • This report aims to highlight the diagnostic challenges of Fluid Overload-associated Large B-Cell Lymphoma (FO-LBCL).
  • Described a case of a 79-year-old man with acute dyspnea due to massive pleural effusion.
  • Diagnostic evaluation included CT scan, PET-CT, pleural fluid cytology, immunophenotyping, and molecular analysis.
  • Patient received R-CHOP-based immunochemotherapy.
  • Diagnosis confirmed as FO-LBCL based on cytology and immunophenotyping characteristics.
  • Patient remains clinically stable post-therapy, showing no systemic progression.
  • Integrated analyses proved crucial in distinguishing FO-LBCL from other lymphomas.

Abstract

BACKGROUND: Fluid Overload-associated Large B-Cell Lymphoma (FO-LBCL) is one of the newly added entities in the WHO classification of Haematolymphoid Tumors 5th edition 1. Formerly, these cases were classified as primary effusion lymphoma-like (effusion) lymphoma (PEL-like (effusion) lymphoma) or HHV8-unrelated PEL-like lymphoma. As knowledge grew regarding the differences in clinical presentation and prognosis of these entities, the need for a distinct classification became apparent. METHOD: We describe a case of a 79-year-old man with acute dyspnea and cough due to massive pleural effusion, revealed by CT scan of the thorax. Further diagnostic evaluation with PET-CT showed no detectable tumor mass apart from the pleural fluid. Pleural fluid cytology revealed numerous large atypical lymphoid cells. Flow cytometric immunophenotyping showed a predominant monoclonal CD19+/CD20+ B-cell population with light chain restriction and CD5 expression. Molecular analysis demonstrated partial clonality, and cytogenetics revealed a complex hyperdiploid karyotype. EBV in situ hybridization and testing for HHV8 and HIV were negative. No underlying immunodeficiency or systemic disease was identified. RESULTS AND CONCLUSION: Based on these findings, diagnosis was most consistent with FO-LBCL, but distinction from other HHV8-negative effusion-based large B-cell lymphomas remains challenging due to overlapping features. The patient received R-CHOP-based immunochemotherapy and remains clinically stable without systemic progression. This case highlights the critical role of integrated cytologic, immunophenotypic, molecular, and virological analyses in establishing the correct classification of effusion-based large B-cell lymphomas and underscores the diagnostic challenges posed by this emerging entity. Accurate recognition of FO-LBCL is essential, as its clinical behavior and therapeutic implications differ from other effusion-based lymphomas.

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Cite This Study

Magalie et al. (2026) studied this question.

synapsesocial.com/papers/6a0172233a9f334c28272389https://doi.org/10.1002/jcla.70244
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