TY - JOUR
T1 - Acquired chromosome rearrangements, including fine interstitial deletions, in a patient with Down syndrome and monoblastic leukemia
AU - Misawa, S.
AU - Testa, J. R.
AU - Strauss, L. C.
AU - Leavitt, R. D.
AU - Civin, C. I.
PY - 1984
Y1 - 1984
N2 - A female child with Down syndrome who developed acute monoblastic leukemia is reported. Anemia associated with milk leukopenia was first recognized when the patient was 14 months old. Acute monoblastic leukemia was diagnosed 1 year later; cytogenetic studies were performed on circulating leukemic cells at this time. Analysis of elongated, finely banded chromosomes revealed three structural rearrangements, including two rather subtle interstitial deletions, in addition to trisomy 21 which was representative of the patient's constitutional karyotype. The karyotype of the leukemic cells was 47,XX,+21,t(3;18)(p23;q11.2), del(7)(q31.1q31.3), del(9)(p22p24 or p21p23). The patient received no cytostatic chemotherapy and died 4 months after the diagnosis of acute leukemia was made.
AB - A female child with Down syndrome who developed acute monoblastic leukemia is reported. Anemia associated with milk leukopenia was first recognized when the patient was 14 months old. Acute monoblastic leukemia was diagnosed 1 year later; cytogenetic studies were performed on circulating leukemic cells at this time. Analysis of elongated, finely banded chromosomes revealed three structural rearrangements, including two rather subtle interstitial deletions, in addition to trisomy 21 which was representative of the patient's constitutional karyotype. The karyotype of the leukemic cells was 47,XX,+21,t(3;18)(p23;q11.2), del(7)(q31.1q31.3), del(9)(p22p24 or p21p23). The patient received no cytostatic chemotherapy and died 4 months after the diagnosis of acute leukemia was made.
KW - Child, Preschool
KW - Chromosome Deletion
KW - Chromosomes, Human, 1-3
KW - Chromosomes, Human, 16-18
KW - Chromosomes, Human, 6-12 and X
KW - Down Syndrome/complications
KW - Female
KW - Humans
KW - Karyotyping
KW - Leukemia, Monocytic, Acute/complications
KW - Splenomegaly/etiology
KW - Translocation, Genetic
UR - https://www.scopus.com/pages/publications/0021721915
UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=purepublist2023&SrcAuth=WosAPI&KeyUT=WOS:A1984TV26500008&DestLinkType=FullRecord&DestApp=WOS
M3 - Article
C2 - 6239138
SN - 0031-4005
VL - 74
SP - 1029
EP - 1033
JO - Pediatrics
JF - Pediatrics
IS - 6
ER -