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A case of CD138-/CD19+/CD4+ IgD plasma cell leukemia
Marc Sorigue1, Jordi Juncà, Susanna Gassiot
1IJC, Hospital Germans Trias i Pujol, Hematology Laboratory and Pathology Service, Badalona, Spain.
This study details an unusual case of IgD plasma cell leukemia (PCL) with a CD138-/CD19+/CD4+ phenotype. Despite atypical findings, immunophenotyping aids in diagnosing challenging PCL cases.
Area of Science:
- Hematology
- Oncology
- Clinical Cytometry
Background:
- Plasma cell leukemia (PCL) is a rare and aggressive hematologic malignancy.
- It involves clonal proliferation of atypical plasma cells, sharing some features with multiple myeloma (MM).
- This report focuses on a unique IgD PCL case with an aberrant immunophenotype.
Observation:
- A 37-year-old patient presented with aggressive plasma cell dyscrasia.
- Peripheral blood and bone marrow samples were analyzed using morphology, flow cytometry, and immunohistochemistry.
- PCL diagnostic criteria were met based on peripheral blood analysis.
Findings:
- Flow cytometry and immunohistochemistry revealed a CD138-/CD38+/CD19+/CD4+/CD56-/CD117- phenotype.
- This immunophenotype is highly unusual for plasma cell leukemia.
- The cells were CD138 negative, CD19 positive, and CD4 positive.
Implications:
- Immunophenotyping is crucial for diagnosing challenging PCL cases.
- Atypical findings, such as the CD138-/CD19+/CD4+ phenotype, should not impede PCL diagnosis.
- Accurate diagnosis relies on integrating immunophenotypic data with clinical and morphological findings.
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