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Immunophenotyping pediatric leukemias in Kelantan, Malaysia
B S Menon1, A Dasgupta, N Jackson
1Department of Paediatrics, School of Medical Sciences, University Sains Malaysia, Kelantan, Malaysia. bina@kb.usm.my
Pediatric Hematology and Oncology
|May 21, 1998
Summary
This study analyzed immunophenotyping in pediatric acute leukemia in Malaysia, finding acute lymphoblastic leukemia (ALL) more common than acute myeloblastic leukemia (AML). The research details cell origins and markers for both leukemia types.
Area of Science:
- Pediatric Hematology
- Immunophenotyping
- Leukemia Research
Background:
- Acute leukemia is a significant health concern in children.
- Immunophenotyping is crucial for classifying leukemia subtypes.
- Data on pediatric acute leukemia in Malaysia is limited.
Purpose of the Study:
- To review immunophenotyping results of pediatric acute leukemia cases in Kelantan, Malaysia.
- To characterize the immunophenotypic profiles of acute lymphoblastic leukemia (ALL) and acute myeloblastic leukemia (AML) in children.
- To determine the incidence of mixed-lineage leukemias.
Main Methods:
- Retrospective review of 45 pediatric acute leukemia cases diagnosed between January 1994 and June 1997.
- Analysis of immunophenotyping data, including cell lineage and marker expression (CD10, CD33, CD13).
- Classification based on World Health Organization (WHO) or similar criteria.
Main Results:
- Acute lymphoblastic leukemia (ALL) accounted for 80% of cases, while acute myeloblastic leukemia (AML) comprised 20%.
- In ALL cases, 3% were B-cell and 22% were T-cell origin; 96% of B-lineage ALL were CD10 positive.
- All AML cases expressed CD33, and 78% were positive for CD13. Mixed-lineage leukemias were observed in 13.8% (My+ ALL) and 11.1% (Ly+ AML).
Conclusions:
- Immunophenotyping is essential for accurate diagnosis and classification of acute leukemia in children.
- The study provides valuable data on the immunophenotypic characteristics of pediatric ALL and AML in a Malaysian population.
- Further research is needed to understand the implications of mixed-lineage leukemias.