Brief Report: A Cytogenetic Study of Acute Erythroleukemia in Children

Author:

DYMENT PAUL G.12,MELNYK JOHN13,BRUBAKER CHARLES A.14

Affiliation:

1. Division of Hematology and the Cytogenetics Unit of the Childrens Hospital of Los Angeles, and the Department of Pediatrics, University of Southern California School of Medicine.

2. University of Southern California School of Medicine. Present Address: Division of Hematology, Childrens Hospital of Los Angeles, P. O. Box 54700, Terminal Annex, Los Angeles, Calif.

3. University of Southern California School of Medicine.

4. University of Southern California School of Medicine; at present: Chief of Pediatric Hematology and Pediatric Cancer Chemotherapy, Cedars-Sinai Medical Center, and Assistant Professor of Pediatrics, University, of California at Los Angeles School of Medicine.

Abstract

Abstract Three children with acute erythroleukemia were studied for chromosomal changes. Two of them had persistently normal karyotypes despite relapse. The third patient was missing a C chromosome, and had 45/46 mosaicism in the bone marrow and a dichotomy between blood (mode of 46) and bone marrow (mode of 45). All of these abnormalities were only evident when he was in relapse. Following partial remission induced with cytosine arabinoside, all subsequent analyses were normal. This is the third case reported of a child with erythroleukemia with aneuploidy in the C group of the chromosomes.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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