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Updated: May 12, 2026

Isolation of CD4+ T-cells and Analysis of Circulating T-follicular Helper (cTfh) Cell Subsets from Peripheral Blood Using 6-color Flow Cytometry
Published on: January 7, 2019
Difficulty in classifying a B cell chronic lymphoproliferative disorder CD5+.
Anamaria Iova1, Ana-Maria Vladareanu, Daniela Vasile
1Department of Hematology, Emergency Universitary Hospital Bucharest, "Carol Davila" University of Medicine and Pharmacy, Bucharest.
This case study details a 53-year-old woman with splenic marginal zone lymphoma. Initial symptoms and tests suggested mantle cell lymphoma, but further analysis revealed a blastoid variant of small lymphocytic lymphoma.
Area of Science:
- Hematology
- Oncology
- Immunohistochemistry
Background:
- Splenic marginal zone lymphoma with plasmacytic differentiation presents unique diagnostic challenges.
- Accurate subtyping of non-Hodgkin lymphomas is crucial for appropriate treatment strategies.
Observation:
- A 53-year-old woman presented with asthenia, significant weight loss, and disorientation.
- Clinical examination revealed lymphadenopathy, hepatomegaly, and splenomegaly.
- Flow cytometry showed a clonal lymphocyte population with specific immunophenotypic markers.
Findings:
- Initial suspicion of mantle cell lymphoma was excluded by bone marrow biopsy and absence of cyclin D1.
- Immunohistochemical analysis and histopathology suggested a blastoid variant of small lymphocytic lymphoma.
- The case highlights the importance of comprehensive diagnostic workup in complex lymphoma cases.
Implications:
- This case underscores the diagnostic difficulties in differentiating lymphoma subtypes.
- Accurate diagnosis impacts patient prognosis and therapeutic decisions.
- Further research into the immunophenotypic profiles of rare lymphoma variants is warranted.
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