The genetic characterization of acute promyelocytic leukemia with cryptic t(15;17) including a new recurrent additional cytogenetic abnormality i(17)(q10)

Author:

Kim M,Lim J,Kim Y,Han K,Lee D H,Chung N G,Cho B,Kim H K,Eom K S,Min C-K,Min W-S

Publisher

Springer Science and Business Media LLC

Subject

Oncology,Cancer Research,Hematology

Reference7 articles.

1. Jaffe E, Harris N, Stein H, Wardiman J . World Health Organization Classification of Tumours. Pathology and Genetics of Tumours of Haematopoietic and Lymphoid Tissues. IARC Press: Lyon, 2001, pp 84–86.

2. Grimwade D, Biondi A, Mozziconacci M-J, Hagemeijer A, Berger R, Neat M et al. Characterization of acute promyelocytic leukemia cases lacking the classic t(15;17): results of the European Working Party. Blood 2000; 96: 1297–1308.

3. Sainty D, Liso V, Cantù-Rajnoldi A, Head D, Mozziconacci M-J, Arnoulet C et al. A new morphological classification system for acute promyelocytic leukemia distinguishes cases with underlying PLZF/RARA rearrangements. Blood 2000; 96: 1287–1296.

4. Tchinda J, Volpert S, Liersch R, Zühlsdorf M, Serve H, Neumann T et al. A cryptic insertion (17;15) on both chromosomes 17 with lack of PML-RARA expression in a case of atypical acute promyelocytic leukemia. Leukemia 2004; 18: 183–186.

5. Lee G, Christina S, Tien S, Ghafar A, Hwang W, Lim L et al. Acute promyelocytic leukemia with PML–RARA fusion on i(17q) and therapy-related acute myeloid leukemia. Cancer Genet Cytogenet 2005; 159: 129–136.

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