Literature DB >> 19998064

Persistence of derivative chromosome 22 after achieving a major molecular response in chronic myeloid leukemia with a cryptic BCR-ABL1 fusion gene.

Hiromichi Matsushita1, Atsuko Masukawa2, Satoshi Arakawa2, Yoshiaki Ogawa3, Satomi Asai4, Miharu Yabe4, Kiyoshi Ando3, Hayato Miyachi4.   

Abstract

We herein report the findings of a 47-year-old Japanese female with chronic myeloid leukemia (CML) with a cryptic BCR-ABL1 transcript on chromosome 9 and a derivative chromosome 22 unrelated to BCR-ABL1. Although she achieved and continued to demonstrate a major molecular response to imatinib treatment following interferon-alpha, there was persistence of a derivative chromosome 22. A detailed chromosome/molecular studies, including serial karyotyping analysis, finally resulted in the karyotyping at the disease onset to be 47,XX,+del(22)(q11.2), with two genetic evens, namely a cryptic BCR-ABL1 transcript on chromosome 9 and derivative chromosome 22 unrelated to BCR-ABL1. This CML case with these two rare genetic events thus raises diagnostic issues such as the difficulty in making a concise evaluation of the chromosomal/molecular events and an accurate disease prognosis, as well as the difficulty in determining the disease remission status after treatment.

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 19998064     DOI: 10.1007/s12185-009-0448-5

Source DB:  PubMed          Journal:  Int J Hematol        ISSN: 0925-5710            Impact factor:   2.490


  22 in total

1.  Clonal Ph-negative hematopoiesis in CML after therapy with imatinib mesylate is frequently characterized by trisomy 8.

Authors:  M K Andersen; J Pedersen-Bjergaard; L Kjeldsen; I H Dufva; K Brøndum-Nielsen
Journal:  Leukemia       Date:  2002-07       Impact factor: 11.528

2.  De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: clinical significance and distribution of breakpoints.

Authors:  D Warburton
Journal:  Am J Hum Genet       Date:  1991-11       Impact factor: 11.025

Review 3.  Chronic myelogenous leukemia: laboratory diagnosis and monitoring.

Authors:  Y L Wang; A Bagg; W Pear; P C Nowell; J L Hess
Journal:  Genes Chromosomes Cancer       Date:  2001-10       Impact factor: 5.006

4.  Der(22) syndrome and velo-cardio-facial syndrome/DiGeorge syndrome share a 1.5-Mb region of overlap on chromosome 22q11.

Authors:  B Funke; L Edelmann; N McCain; R K Pandita; J Ferreira; S Merscher; M Zohouri; L Cannizzaro; A Shanske; B E Morrow
Journal:  Am J Hum Genet       Date:  1999-03       Impact factor: 11.025

5.  Genomewide screening of DNA copy number changes in chronic myelogenous leukemia with the use of high-resolution array-based comparative genomic hybridization.

Authors:  Noriko Hosoya; Masashi Sanada; Yasuhito Nannya; Kumi Nakazaki; Lili Wang; Akira Hangaishi; Mineo Kurokawa; Shigeru Chiba; Seishi Ogawa
Journal:  Genes Chromosomes Cancer       Date:  2006-05       Impact factor: 5.006

6.  Chromosomal, morphological and clinical correlations in blastic crisis of chronic myeloid leukaemia: a study of 69 cases.

Authors:  G Alimena; B Dallapiccola; R Gastaldi; F Mandelli; L Brandt; F Mitelman; P G Nilsson
Journal:  Scand J Haematol       Date:  1982-02

7.  Persistence of chromosomal abnormalities additional to the Philadelphia chromosome after Philadelphia chromosome disappearance during imatinib therapy for chronic myeloid leukemia.

Authors:  Alfonso Zaccaria; Anna Maria Valenti; Emilio Donti; Alessandro Gozzetti; Sonia Ronconi; Francesco Spedicato
Journal:  Haematologica       Date:  2007-04       Impact factor: 9.941

8.  Translocation of BCR to chromosome 9 in a Philadelphia-negative chronic myeloid leukemia.

Authors:  V Brunel; D Sainty; R Costello; M J Mozziconacci; J Simonetti; C Arnoulet; L Coignet; R Bouabdallah; J A Gastaut; J Gabert
Journal:  Cancer Genet Cytogenet       Date:  1995-11

9.  Translocation of BCR to chromosome 9: a new cytogenetic variant detected by FISH in two Ph-negative, BCR-positive patients with chronic myeloid leukemia.

Authors:  A Hagemeijer; A Buijs; E Smit; B Janssen; G J Creemers; D Van der Plas; G Grosveld
Journal:  Genes Chromosomes Cancer       Date:  1993-12       Impact factor: 5.006

10.  Partial trisomy of chromosome 22 resulting from a supernumerary marker chromosome 22 in a child with features of cat eye syndrome.

Authors:  Valérie Bélien; Marion Gérard-Blanluet; Stéphane Serero; Nathalie Le Dû; Clarisse Baumann; Marie-Line Jacquemont; Céline Dupont; Kada Krabchi; Séverine Drunat; Annie Elbez; Jean-Claude Janaud; Brigitte Benzacken; Alain Verloes; Anne-Claude Tabet; Azzedine Aboura
Journal:  Am J Med Genet A       Date:  2008-07-15       Impact factor: 2.802

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.