Background: Chronic lymphoproliferative disorders (CLPD) are a group of lymphatic malignancies characterized by proliferation of neoplastic mature lymphocytes, and may be sourced B, T and natural killer cells (NK). Flow cytometric (FC) immunophenotyping is a routine practice in the differential diagnosis of these tumors, contributing to greater accuracy and new therapeutic perspectives. Methods: Patients (n = 500) with CLPD were assessed by FC. In addition, we gathered patient information such as age, sex and hematologic data. Results: The results showed that 86.6% of cases were B-cell and 13.4% T/NK CLPD. B-cell CLPD distribution was as follows: 265 B-cell chronic lymphocytic leukemia, 17 B-cell prolymphocytic leukemia, 11 hairy cell leukemia, 3 follicular lymphoma in leukemic phase, 3 splenic lymphoma with villous lymphocytes, 12 mantle cell lymphoma, one Waldenstrong macroglobulinemia, 47 multiple myeloma, 12 plasma cell leukemia, 9 Burkitt lymphoma and 37 B-cell CLPD with non-specific immunoclassification. The T/NK CLPD classifications were as follows: 11 large granular lymphocyte leukemia, 14 T-cell prolymphocytic leukemia, 10 adult T-cell leukemia lymphoma, 8 Sézary syndrome and 24 T-cell peripheral lymphoma. Conclusion: The data suggest that immunophenotyping is an important method in diagnosis, monitoring and prognosis when determining the pathological mechanisms of CLPD evolution.

Disclosures

No relevant conflicts of interest to declare.

Author notes

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Asterisk with author names denotes non-ASH members.

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