IGHCCND1 MANTLE CELL LYMPHOMA,BLOOD & BONE MARROW

This test detects the t(11;14) translocation involving the IGH/CCND1 genes, mainly observed in mantle cell lymphoma. It is used to confirm diagnosis and guide treatment in suspected mantle cell lymphoma cases. The test is typically performed on blood and bone marrow samples.

Also known asIgh/ccnd1 Mantle Cell LymphomaBlood & Bone Marrow Igh/ccnd1 Mantle Cell LymphomaBlood & Bone Marrow

Available via

Home Collection, Lab Visit

Contains

4 parameters

Earliest reports in

7 Working Days

Test details

IGHCCND1 MANTLE CELL LYMPHOMA,BLOOD & BONE MARROW Test in Vadodara Overview

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?

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?

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.

More Information

Other Names: IGH/CCND1 Fusion Gene Test, t(11;14)(q13;q32) Translocation Study, Mantle Cell Lymphoma FISH Panel, Cyclin D1 Rearrangement Test

 

Mantle Cell Lymphoma (MCL) is a rare and aggressive type of B-cell non-Hodgkin lymphoma that arises from B lymphocytes in the “mantle zone” of lymphoid follicles. It accounts for about 5–7% of all non-Hodgkin lymphomas and primarily affects older adultsMantle cell lymphoma is considered aggressive but may have variable clinical behavior, with some patients showing slower progression (indolent forms).

Preparations

No special preparations needed

Test included
IGHCCND1 MANTLE CELL LYMPHOMA,BLOOD & BONE MARROW includes 4 parameters

  • Specimen
  • Clinical Indications
  • Total Number Of Cells Analysed
  • Interpretation

Test code

6039F

Specimen vol. and vacutainer information
SpecimenVacutainerVolume
Bone MarrowOthers
Heparin Whole BloodGreen Vacutainer

Specimen stability information

Bone Marrow, Heparin Whole Blood

Collection instructions

Age,Gender,Clinical history required

Specimen rejection criteria

Test run frequency

Every Day TIME - 07:00

Turn around time

7 Working Days

Performing locations

Department

  • Cytogenetics

CPT and Loinc codes

IGHCCND1 MANTLE CELL LYMPHOMA,BLOOD & BONE MARROW

4500