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Parotid gland follicular lymphoma lacking both cytoplasmic and surface light chains: a rare case
Jenny Smith1, Fang Wen2, Jeffrey Cao3
1Department of Pathology, Loma Linda University Loma Linda, CA.
Insights
Immunoglobulin light chain (LC) restriction is a key marker for B-cell non-Hodgkin lymphoma (B-NHL). This study reports a rare B-NHL case lacking both cytoplasmic and surface LCs, highlighting diagnostic challenges.
Area of Science:
- Hematology
- Oncology
- Immunology
Background:
- Immunoglobulin light chain (LC) restriction is a standard diagnostic marker for B-cell non-Hodgkin lymphoma (B-NHL) using flow cytometric immunophenotyping (FCI).
- A small subset of mature B-NHLs are known to lack surface LC, but deficiency in both cytoplasmic and surface LCs is exceedingly rare.
Observation:
- This report details a case of primary parotid gland follicular lymphoma in a 63-year-old male patient.
- The lymphoma cells in this case exhibited a deficiency of both cytoplasmic and surface LCs.
Findings:
- A more sensitive FCI method, utilizing a combination of monoclonal and polyclonal anti-LC antibodies, was employed.
- This advanced technique confirmed the absence of LCs in the lymphoma cells, a finding previously reported in only three B-NHL cases.
Implications:
- The absence of LCs presents a significant diagnostic pitfall for initial B-NHL diagnosis.
- This immunophenotypic aberrancy also poses challenges for the accurate detection of minimal residual disease.
- Awareness of this rare finding is crucial for accurate diagnosis and patient management in hematologic malignancies.
Abstract:
Immunoglobulin light chain (LC) restriction is detected in the majority of B-cell non-Hodgkin lymphoma (B-NHL) by flow cytometric immunophenotyping (FCI) and serves as a surrogate marker of monoclonality. Even though it is known a small percentage of mature B-NHLs lacking surface LC, deficiency of both cytoplasmic and surface LCs has been reported in only three B-NHL cases. We report a primary parotid gland follicular lymphoma in a 63-year-old man and the lymphoma cells were deficient of cytoplasmic/surface LCs. Compared to previous reports, we used a more sensitive FCI method by combining both monoclonal and polyclonal anti-LC antibodies. Lacking LCs poses as a pitfall for the initial diagnosis of B-NHL, as well as for detecting minimal residual disease. It is important to be aware of this rare immunophenotypic aberrancy.
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