Korean J Lab Med.  2009 Oct;29(5):396-401. 10.3343/kjlm.2009.29.5.396.

Discrepant Immunophenotypic Characteristics between the Lymph Node and Bone Marrow in Two Mixed-Phenotype Acute Leukemia Patients

Affiliations
  • 1Department of Laboratory Medicine & Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea. sunnyhk@skku.edu
  • 2Department of Diagnostic Pathology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.

Abstract

The immunophenotypic profile of hematological malignancies is usually consistent among different sites of involvement; this consistency allows reliable diagnosis from peripheral blood, bone marrow, or lymph node, especially in cases of acute leukemia. Although in a minority of lymphoma patients, two or more different populations with discordant immunophenotypes have been described, either at the same or distinct sites. Here, we report two Korean patients with acute leukemia where the results of immunophenotypic analysis of the bone marrow specimen were different from those of immunohistochemical studies of a biopsy sample of a cervical lymph node, particularly with respect to myeloperoxidase and CD3. The clinical significance of the immunophenotypic disparity found in the patients still remains unknown; however, discrepancies between the different anatomic sites that are simultaneously involved can occur in a subset of leukemia patients. Therefore, integration of all the relevant results, including those of the bone marrow studies, may be helpful for accurate diagnosis and selecting appropriate treatment modalities.

Keyword

Mixed-Phenotype Acute Leukemia; Lymph node; Bone marrow; Immunophenotype

MeSH Terms

Acute Disease
Adolescent
Adult
Antigens, CD3/metabolism
Bone Marrow/*pathology
Female
Flow Cytometry
Humans
Immunophenotyping/*methods
Leukemia/*diagnosis/pathology
Lymph Nodes/*pathology
Male
Peroxidase/metabolism
Phenotype

Figure

  • Fig. 1. Patient 1. (A) Cervical lymph node biopsy showing almost complete replacement by malignant cells (H&E stain, ×400). (B) Bone marrow aspirate smear showing blast cells with rather abundant cytoplasm with granules (Wright-Giemsa stain, ×1,000). (C, D) Immunohistochemical stains on lymph node biopsy. The majority of neoplastic cells are strongly positive for CD3 (C) and TdT (D) (×1,000). (E, F) Immunohistochemical stains on bone marrow biopsy. The majority of neoplastic cells are negative for CD3 (E) and TdT (F) (×1,000). (G) Flow cytometric immunophenotyping of the marrow blasts showing negative expression of CD3 and TdT. Abbreviation: Tdt, terminal deoxynucleotidyl transferase.

  • Fig. 2. Patient 2. (A) Cervical lymph node biopsy showing diffuse infiltration by neoplastic cells (H&E stain, ×400). (B) Bone marrow aspirate smear showing blast cells (arrows) with high nucleus/cytoplasm ratio and prominent nucleoli (Wright-Giemsa stain, ×1,000). (C) Immunohistochemical stain on lymph node biopsy. The large neoplastic cells showed positivity to MPO (×1,000). (D) Immunohistochemical stain on bone marrow biopsy. The neoplastic cells showed negativity to MPO (×1,000). (E) Flow cytometric immunophenotyping of the marrow blasts showing negative expression of MPO. Abbreviation: MPO, myeloperoxidase.


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