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Bioprinting of Hydrogel Tumor Slices as a 3D Model for Mantle Cell Lymphoma
Published on: September 12, 2025
BCL6, MUM1, and CD10 expression in mantle cell lymphoma
Gabriela Gualco1, Lawrence M Weiss, William J Harrington
1Consultoria em Patologia, Botucatu, SP, Brazil.
Applied Immunohistochemistry & Molecular Morphology : AIMM
|October 15, 2009
Summary
Aberrant immunophenotypes in mantle cell lymphoma (MCL) are infrequent but occur. While most MCL cases express CD20, CD5, and cyclin-D1 with t(11;14), variations in CD10, BCL-6, and MUM1 expression are noted.
Area of Science:
- Hematology
- Oncology
- Immunophenotyping
Background:
- Mantle cell lymphoma (MCL) typically expresses CD20, CD5, and cyclin-D1, with the characteristic t(11;14) translocation.
- Germinal center cell markers are usually absent in MCL, though aberrant phenotypes like CD5-negative or cyclin-D1-negative MCL have been reported.
- Limited cases of MCL with CD10 and/or BCL-6 expression exist.
Purpose of the Study:
- To determine the frequency of aberrant immunophenotypes, including CD10, BCL-6, and MUM1 expression, in a cohort of 127 MCL cases.
- To analyze the co-expression patterns of BCL-6, MUM1, and CD10 in MCL.
- To evaluate the diagnostic implications of aberrant phenotypes in MCL.
Main Methods:
- Immunohistochemical analysis of 127 MCL cases.
- Assessment of CD10, BCL-6, and MUM1 protein expression.
- Correlation of immunophenotypic findings with the characteristic MCL markers (CD20, CD5, cyclin-D1) and t(11;14) translocation.
Main Results:
- All cases were positive for CD20 and cyclin-D1; 96% expressed CD5 and 98% showed t(11;14).
- BCL-6 expression was found in 12% of cases, and MUM1 in 35%.
- CD10 positivity (≥30% neoplastic cells) was absent; only 3 cases showed 10-20% CD10 positivity. MUM1 was expressed in 67% of BCL-6 positive cases.
Conclusions:
- Aberrant immunophenotypes in MCL are infrequent but not rare.
- The presence of aberrant markers like CD10, BCL-6, or MUM1 does not exclude an MCL diagnosis in otherwise typical cases.
- Understanding these variations aids in accurate MCL diagnosis and subclassification.
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