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Updated: Jun 6, 2025

Tumor Engraftment in a Xenograft Mouse Model of Human Mantle Cell Lymphoma
Published on: March 30, 2018
A rapid progression from classical mantle cell lymphoma to a blastoid variant
Radu Chiriac1, Marie Donzel2, Lucile Baseggio1
1Hospices Civils de Lyon, Centre Hospitalier Lyon Sud, Laboratoire d'hématologie biologique, Pierre-Bénite, France.
This case report details an 82-year-old male with mantle cell lymphoma (MCL) that transformed into the aggressive blastoid variant. Despite intensive treatments, the patient experienced disease progression and ultimately died, highlighting the poor prognosis of blastoid MCL.
Area of Science:
- Hematology
- Oncology
- Clinical Case Studies
Background:
- Mantle cell lymphoma (MCL) is a B-cell non-Hodgkin lymphoma.
- The blastoid variant of MCL is associated with a more aggressive clinical course and poorer prognosis.
Observation:
- An 82-year-old male with classical MCL progressed to the blastoid variant with central nervous system (CNS) involvement.
- Initial treatment with oral chemotherapy (PEP-C) and ibrutinib failed to control the disease.
Findings:
- Despite intensive salvage therapy including high-dose cytarabine, rituximab, and intrathecal methotrexate, the patient experienced refractory disease progression.
- The case illustrates the challenges in treating advanced blastoid MCL, particularly with CNS dissemination.
Implications:
- Blastoid MCL, especially with CNS involvement, presents a significant therapeutic challenge with a dismal outcome.
- There is a critical need for novel therapeutic strategies and effective CNS prophylaxis in managing aggressive MCL variants.
- Individualized treatment approaches are essential for patients with refractory or advanced-stage MCL.
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