Literature DB >> 17189222

Acute myelomonocytic leukemia with dysplastic bone marrow eosinophils showing t(5;17)(q13;q11) and a secondary chromosomal aberration, inv(16)(p13q22).

Rika Sakai1, Katsumichi Fujimaki, Etsuko Yamazaki, Hiroshi Sakamoto, Heiwa Kanamori, Ikuo Miura, Yoshiaki Ishigatsubo.   

Abstract

inv(16)(p13q22) is associated with de novo acute myelomonocytic leukemia with dysplastic bone marrow eosinophils (AMML Eo), which has a relatively favorable clinical course with a longer remission duration and better survival prospects. On the other hand, t(5; 17)(q13;q11), although relatively rare, has been reported to be a component of complex chromosomal abnormalities in myelodysplastic syndromes and secondary acute myeloid leukemia (AML). We treated a 29-year-old woman with the first reported case of de novo AMML Eo with inv(16)(p13q22) in addition to t(5; 17)(q13;q11). Although she attained complete remission (CR) immediately after induction therapy, the disease recurred 1 year after the completion of consolidation therapies. She underwent HLA-matched unrelated allogeneic bone marrow transplantation (UBMT), together with a myeloablative conditioning regimen, after achieving a second CR and has survived without a recurrence for more than 24 months since UBMT. In general, certain secondary chromosomal abnormalities are associated with the phenotype of the disease, which retains its essential biologic characteristics established by the primary abnormality. Accordingly, the primary nature of the leukemic cells in this case differs from the findings for core-binding factor AML with inv(16)(p13q22). We believe this report is the first of de novo AMML Eo with t(5; 17)(q13;q11) showing as a secondary chromosomal aberration with inv(16)(p13q22).

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Year:  2006        PMID: 17189222     DOI: 10.1532/IJH97.06054

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


  17 in total

1.  Prognostic factors and outcome of core binding factor acute myeloid leukemia patients with t(8;21) differ from those of patients with inv(16): a Cancer and Leukemia Group B study.

Authors:  Guido Marcucci; Krzysztof Mrózek; Amy S Ruppert; Kati Maharry; Jonathan E Kolitz; Joseph O Moore; Robert J Mayer; Mark J Pettenati; Bayard L Powell; Colin G Edwards; Lisa J Sterling; James W Vardiman; Charles A Schiffer; Andrew J Carroll; Richard A Larson; Clara D Bloomfield
Journal:  J Clin Oncol       Date:  2005-08-20       Impact factor: 44.544

2.  Inversion of chromosome 16 and dysplastic eosinophils in accelerated phase of chronic myeloid leukemia.

Authors:  H Enright; D Weisdorf; L Peterson; R E Rydell; M E Kaplan; D C Arthur
Journal:  Leukemia       Date:  1992-05       Impact factor: 11.528

3.  Analysis of complex chromosomal rearrangements in adult patients with MDS and AML by multicolor FISH.

Authors:  Libuse Babicka; Sarka Ransdorfova; Jana Brezinova; Zuzana Zemanova; Lenka Sindelarova; Magda Siskova; Jacqueline Maaloufova; Jaroslav Cermak; Kyra Michalova
Journal:  Leuk Res       Date:  2006-05-09       Impact factor: 3.156

4.  Acute myelomonocytic leukemia with inv(16)(p13q22) complicating Philadelphia chromosome positive chronic myeloid leukemia.

Authors:  S Heim; B E Christensen; T Fioretos; A G Sørensen; N T Pedersen
Journal:  Cancer Genet Cytogenet       Date:  1992-03

5.  Inversion of chromosome 16 and bone marrow eosinophilia in a myelomonocytic transformation of chronic myeloid leukemia.

Authors:  N Asou; I Sanada; K Tanaka; M Hidaka; H Suzushima; H Matsuzaki; F Kawano; K Takatsuki
Journal:  Cancer Genet Cytogenet       Date:  1992-07-15

6.  SSBP2, a candidate tumor suppressor gene, induces growth arrest and differentiation of myeloid leukemia cells.

Authors:  Hong Liang; Susmita Samanta; Lalitha Nagarajan
Journal:  Oncogene       Date:  2005-04-14       Impact factor: 9.867

7.  Mapping of chromosome 17 breakpoints in acute myeloid leukemias.

Authors:  L Longo; E Donti; A Mencarelli; G Avanzi; L Pegoraro; G Alimena; A Tabilio; G Venti; F Grignani; P G Pelicci
Journal:  Oncogene       Date:  1990-10       Impact factor: 9.867

8.  Association of an inversion of chromosome 16 with abnormal marrow eosinophils in acute myelomonocytic leukemia. A unique cytogenetic-clinicopathological association.

Authors:  M M Le Beau; R A Larson; M A Bitter; J W Vardiman; H M Golomb; J D Rowley
Journal:  N Engl J Med       Date:  1983-09-15       Impact factor: 91.245

9.  The importance of diagnostic cytogenetics on outcome in AML: analysis of 1,612 patients entered into the MRC AML 10 trial. The Medical Research Council Adult and Children's Leukaemia Working Parties.

Authors:  D Grimwade; H Walker; F Oliver; K Wheatley; C Harrison; G Harrison; J Rees; I Hann; R Stevens; A Burnett; A Goldstone
Journal:  Blood       Date:  1998-10-01       Impact factor: 22.113

10.  Molecular genetics of myeloid leukemia: identification of the commonly deleted segment of chromosome 20.

Authors:  D Roulston; R Espinosa; M Stoffel; G I Bell; M M Le Beau
Journal:  Blood       Date:  1993-12-01       Impact factor: 22.113

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  1 in total

1.  Idiopathic hypereosinophilia is clonal disorder? Clonality identified by targeted sequencing.

Authors:  Jee-Soo Lee; Heewon Seo; Kyongok Im; Si Nae Park; Sung-Min Kim; Eun Kyoung Lee; Jung-Ah Kim; Joon-Hee Lee; Sunghoon Kwon; Miyoung Kim; Insong Koh; Seungwoo Hwang; Heung-Woo Park; Hye-Ryun Kang; Kyoung Soo Park; Ju Han Kim; Dong Soon Lee
Journal:  PLoS One       Date:  2017-10-31       Impact factor: 3.240

  1 in total

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