A Case of Acute Lymphoblastic Leukemia with ider(9)(q10)t(9;22)(q34;q11.2)
Author(s) -
Jungwon Huh,
Wha-Soon Chung
Publication year - 2006
Publication title -
annals of laboratory medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.784
H-Index - 34
eISSN - 2234-3814
pISSN - 2234-3806
DOI - 10.3343/kjlm.2006.26.3.223
Subject(s) - isochromosome , derivative chromosome , fluorescence in situ hybridization , chronic myelogenous leukemia , leukemia , abl , breakpoint cluster region , biology , chromosome , microbiology and biotechnology , karyotype , cancer research , medicine , immunology , genetics , gene , receptor , tyrosine kinase
ider(9)(q10)t(9;22)(q34;q11.2) is an isochromosome for the long arm of a derivative chromosome 9 generated by a t(9;22), resulting from the deletion of the short arm of chromosome 9. It is known to be rarely observed in acute lymphoblastic leukemia (ALL) or lymphoblastic crisis transformed from chronic myelogenous leukemia. We herein describe a 26-year-old female patient with precursor B-cell ALL, cytogenetically characterized by ider(9)(q10)t(9;22). Fluorescence in situ hybridization analysis showed two ABL-BCR fusion signals on the derivative chromosome 9 and one BCR-ABL fusion signal on the derivative chromosome 22. Although a t(9;22) and a deletion of the short arm of chromosome 9 are known to be associated with a poor prognostic factor in acute lymphoblastic leukemia, a larger study is needed to determine the prognosis of ider(9)(q10)t(9;22) cases.
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