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Tumor Engraftment in a Xenograft Mouse Model of Human Mantle Cell Lymphoma
Published on: March 30, 2018
Expression of LEF1 in mantle cell lymphoma
Dennis P O'Malley1, John P Lee2, Andrew M Bellizzi2
1Neogenomics, Aliso Viejo, CA, United States; Department of Hematopathology, M.D. Anderson Cancer Center/University of Texas, Houston, TX, United States.
Insights
LEF1 staining is a useful marker for differentiating small lymphocytic lymphoma/chronic lymphocytic leukemia (CLL/SLL) from mantle cell lymphoma (MCL). However, rare cases of MCL can express LEF1, posing a diagnostic challenge.
Area of Science:
- Hematology
- Oncology
- Pathology
Background:
- Small lymphocytic lymphoma/chronic lymphocytic leukemia (CLL/SLL) and mantle cell lymphoma (MCL) are distinct lymphoid neoplasms.
- Diagnostic differentiation is crucial for appropriate patient management.
- LEF1 immunohistochemistry is highly sensitive for CLL/SLL, with rare reports in MCL.
Observation:
- An index case of mantle cell lymphoma (MCL) with cyclin D1 expression and t(11;14) translocation was found to express LEF1.
- LEF1 expression was assessed in 23 MCL cases, with one additional positive case identified.
- Literature review suggests a 4-9% frequency of LEF1 expression in MCL.
Findings:
- LEF1 expression in MCL is unusual but occurs rarely.
- LEF1 positivity in MCL can mimic CLL/SLL, creating a diagnostic pitfall.
- Immunohistochemical markers like cyclin D1 and SOX11 remain essential for MCL diagnosis.
Implications:
- LEF1 should be interpreted cautiously in the differential diagnosis of MCL.
- Awareness of LEF1 expression in MCL aids accurate diagnosis and classification.
- Further studies are warranted to understand the biological basis of LEF1 expression in MCL.
Abstract:
Small lymphocytic lymphoma/chronic lymphocytic leukemia (CLL/SLL) and mantle cell lymphoma (MCL) usually are distinctly different in regard to clinical presentation, morphology, immunophenotype and molecular/genetic findings. In spite of this, select cases may show overlapping characteristics and represent a diagnostic challenge. Recently LEF1 staining was identified as a fairly characteristic finding in CLL/SLL, with positivity identified in up to 95% of cases. LEF1 staining has not been reported as being present in cases of MCL, making this stain a useful tool in distinguishing these diagnoses. We identified an index case of MCL with cyclin D1 expression and the presence of the typical t(11;14) IGH-CCND1, which expressed LEF1. Subsequently, we assessed LEF1 immunohistochemical staining in a series of 23 cases of MCL, as confirmed by staining for cyclin D1 and/or SOX11. We found expression present in one additional case, and evaluated some published literature suggesting a frequency of 4-9% expression of LEF1 by MCL. LEF1 expression by immunohistochemistry in MCL is unusual but can be seen rarely, and could represent a potential diagnostic pitfall.
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