Ighccnd1 Mantle Cell Lymphoma & Bone Marrow

What is Mantle Cell Lymphoma, IGH/CCND1 test?

Mantle cell lymphoma (MCL), IGH/CCND1 test is a molecular cytogenetic test used to detect the t(11;14)(q13;q32) chromosomal translocation, which fuses the CCND1 (cyclin D1) gene on chromosome 11 with the IGH (immunoglobulin heavy chain) gene on chromosome 14. This translocation leads to overexpression of cyclin D1, a protein that promotes uncontrolled cell proliferation, and is a hallmark feature of mantle cell lymphoma, a type of B-cell non-Hodgkin lymphoma. Mantle cell lymphoma (MCL), IGH/CCND1 test is usually performed using Fluorescence In Situ Hybridization (FISH) on blood or bone marrow samples.

Why consider mantle cell lymphoma, IGH/CCND1 test in Kochi?

Mantle Cell Lymphoma, IGH/CCND1 test can be considered for

• To confirm the diagnosis of mantle cell lymphoma through detection of its characteristic genetic marker.

• To differentiate MCL from other B-cell lymphomas, especially chronic lymphocytic leukemia (CLL) or diffuse large B-cell lymphoma (DLBCL).

• To assess prognosis and predict disease behavior, as cyclin D1 overexpression is associated with aggressive growth.

• To monitor disease progression or response to therapy.

Who should get tested for mantle cell lymphoma, IGH/CCND1 test in Kochi?

Mantle cell lymphoma, IGH/CCND1 test is generally recommended for:

• Patients with suspected or confirmed mantle cell lymphoma.

• Individuals with abnormal lymphocytes in blood or bone marrow suggestive of MCL.

• Cases requiring molecular confirmation of the t(11;14) translocation for diagnosis and treatment planning.

• Patients undergoing risk stratification or monitoring during therapy.

It accounts for about 5–7% of all non-Hodgkin lymphomas and primarily affects older adults. Mantle cell lymphoma is considered aggressive but may have variable clinical behavior, with some patients showing slower progression (indolent forms).