What is it? Chronic Leukemia Panel is a genetic panel used for the molecular analysis of chronic leukemias. The test helps identify genetic and molecular alterations associated with the disease.
What does it analyze? The panel analyzes genetic alterations that may be present in leukemic cells, helping with:
The panel includes a combination of markers that are important for the characterization of B cells, T cells, and plasma cells, including:
When is it recommended? It may be recommended when chronic leukemia is suspected or has been diagnosed, in order to complement the patient's hematological and molecular evaluation.
How is the sample collected? The sample is collected according to the physician's request, usually from peripheral blood or hematological material, and analyzed using advanced molecular technologies.
Analysis The analysis is performed using NGS (Next Generation Sequencing) technology, which enables the identification of genetic alterations relevant to the disease.
Turnaround time The result is processed at the specialized laboratory Neuberg Diagnostics, with the turnaround time depending on the panel protocol.
It is an immunophenotypic panel that uses Flow Cytometry to identify and characterize abnormal hematological cell populations.
It is primarily used in the evaluation of chronic leukemias and lymphoproliferative disorders, particularly those involving B cells.
The panel includes markers such as CD45, CD5, CD10, CD19, FMC7, CD23, CD20, CD22, CD34, CD38, CD56, CD138, CD79b, κ/λ, and others.
Yes. Immunophenotyping by Flow Cytometry is an important part of the evaluation of Chronic Lymphocytic Leukemia (CLL).
Depending on the clinical case, the analysis can be performed using peripheral blood or a bone marrow aspirate.
No. The Chronic Leukemia Panel is an immunophenotypic analysis performed using Flow Cytometry, whereas IgVH (CLL) is a molecular test that determines the mutational status of the IGHV gene.
The results are interpreted together with other hematological tests, clinical findings, and, when necessary, molecular or cytogenetic tests.
The test should be recommended and interpreted by a hematologist based on the patient's medical history and test results.