Korean J Hematol.  2006 Jun;41(2):129-133. 10.5045/kjh.2006.41.2.129.

CD56+ T-cell Prolymphocytic Leukemia Showing a High Expression Level of TCL1 Oncogene: A Case Report with a Review of the Literature

Affiliations
  • 1Department of Laboratory Medicine, Chonnam National University Medical School, Chonnam National University Hwasun Hospital, Korea. mgshin@chonnam.ac.kr
  • 2Genome Research Center for Hematopoietic Disease, Chonnam National University Hwasun Hospital, Korea.
  • 3Department of Laboratory Medicine, Sunchon St. Carollo Hospital, Hwasun, Korea.

Abstract

T-cell prolymphocytic leukemia (T-PLL) is a rare mature post-thymic T-cell malignancy with infiltration to the blood, bone marrow, lymph node, liver, spleen and skin; this disease has a poor prognosis and an aggressive clinical course. We report here on a case of CD56+ T-PLL that was diagnosed by hematological examination, immunophenotyping and molecular studies including determining the TCL1 expression by using reverse-transcriptase polymerase chain reaction (RT-PCR), and direct sequencing of the RT-PCR product.

Keyword

T-cell Prolymphocytic Leukemia; TCL1; CD56

MeSH Terms

Bone Marrow
Immunophenotyping
Leukemia, Prolymphocytic, T-Cell*
Liver
Lymph Nodes
Oncogenes*
Polymerase Chain Reaction
Prognosis
Skin
Spleen
T-Lymphocytes*

Figure

  • Fig. 1 Morphology of T-PLL cells. Peripheral blood (A) and bone marrow aspirate (B) show many small variants of prolymphocytes (Wright stain, ×1000). Bone marrow section (C) shows infiltration of monotonous leukemic cells and hypercellular marrow for age (50%) (H-E stain, ×100).

  • Fig. 2 Expression of the TCL1 gene. The TCL1 gene was abnormally expressed (A) in patient leukemic cells (P), but not in normal blood cells (N); C, β-actin expression; M, marker (100 bp ladder). Partial sequencing chromatogram (B) of RT-PCR products from the patient and NCBI BLAST search show the identical results for the T-cell receptor alpha delta locus (accession No. 000662.1) that juxtapose TCL1 gene. The TCL1 gene maps at chromosome 14q32.1 and is activated in T cell leukemia and lymphomas by either chromosome translocations or inversions that juxtapose the TCL1 gene to the alpha/delta or the beta locus of the T cell receptor.


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