Journal article
Characterization of Immunophenotypic Aberrancies in 200 Cases of B Acute Lymphoblastic Leukemia
American journal of clinical pathology, Vol.132(6), pp.940-949
2009
DOI: 10.1309/AJCP8G5RMTWUEMUU
PMID: 19926587
Abstract
Morphologic distinction of leukemic lymphoblasts in B acute lymphoblastic leukemia (B-ALL) from their nonneoplastic counterparts in bone marrow (hematogones) can be difficult. Thus, the presence of aberrant antigen expression detectable by flow cytometry may be critical for diagnosis of B-ALL and detection of minimal residual disease. The current study examined the immunophenotype of B-lineage leukemic lymphoblasts in 200 consecutive, unique, pretreatment patient specimens. We found that all cases of B-ALL exhibited multiple immunophenotypic aberrancies by which they can be distinguished from hematogones. The most frequent aberrancies were uniform or a spectrum of expression of terminal deoxynucleotidyl transferase and CD34, underexpression of CD45, overexpression of CD10, underexpression of CD38, and underexpression of CD20. Asynchronous coexpression of CD34 and CD20 was also frequently observed. Of the 200 cases, 86.5% expressed myeloid-associated antigens, and 19.0% expressed 3 or more. Of 200 cases, 9.0% aberrantly expressed T cell-associated antigens. There were significant differences in antigen-expression patterns between adult and pediatric B-ALL. Specific aberrancies correlate with recurrent cytogenetic abnormalities in B-ALL.
Details
- Title: Subtitle
- Characterization of Immunophenotypic Aberrancies in 200 Cases of B Acute Lymphoblastic Leukemia
- Creators
- Adam C SEEGMILLER - Department of Pathology, University of Texas Southwestern Medical Center, Dallas, United StatesSteven H KROFT - Department of Pathology, Medical College of Wisconsin, Milwaukee, United StatesNitin J KARANDIKAR - Department of Pathology, University of Texas Southwestern Medical Center, Dallas, United StatesRobert W MCKENNA - Department of Laboratory Medicine and Pathology, University of Minnesota Medical School, Minneapolis, United States
- Resource Type
- Journal article
- Publication Details
- American journal of clinical pathology, Vol.132(6), pp.940-949
- DOI
- 10.1309/AJCP8G5RMTWUEMUU
- PMID
- 19926587
- NLM abbreviation
- Am J Clin Pathol
- ISSN
- 0002-9173
- eISSN
- 1943-7722
- Publisher
- American Society of Clinical Pathologists; Chicago, IL
- Language
- English
- Date published
- 2009
- Academic Unit
- Pathology
- Record Identifier
- 9984047628102771
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