Acute myeloid leukemia with promyelocytic morphology lacking RARA rearrangement and with double minutes, MYC deletion and 2 cell lines with amplification of MYC region: case report and literature review

Author:

Xu Jie,Xenocostas Anargyros,Lazo-Langner Alejandro

Publisher

Springer Science and Business Media LLC

Subject

Hematology,Histology,Pathology and Forensic Medicine

Reference18 articles.

1. Grimwade D, Coco FL (2002) Acute promyelocytic leukemia: a model for the role of molecular diagnosis and residual disease monitoring in directing treatment approach in acute myeloid leukemia. Leukemia 16:1959–1973

2. Kim MJ, Cho SY, Kim MH et al (2010) FISH-negative cryptic PML-RARA rearrangement detected by long-distance polymerase chain reaction and sequencing analyses: a case study and review of the literature. Canc Genet Cytogenet 203:278–283

3. Wakim JJ, Tirado CA (2012) Acute promyelocytic leukemia lacking the classic translocation t(15;17). In: Koschmieder S, Krug U editors. Myeloid leukemia—clinical diagnosis and treatment. ISBN 978-953-307-886-1; InTech. 2012; pp219-234

4. Mozziconacci MJ, Liberator C, Grignai F et al (1999) Atypical response to all-trans retinoic acid in a der(5)t(5;17) acute promyelocytic leukemia. Leukemia 13:862–868

5. Schoch C (2006) M3/M3v acute non lymphocytic leukemia (M3-ANLL); M3/M3v acute myeloid leukemia (AML M3/M3v); acute promyelocytic leukemia (APL). Atlas Genet Cytogenet Oncol Haematol. January 2006 . URL: http://AtlasGeneticsOncology.org/Anomalies/M3ANLLID1240.html . Accessed on Jan 18, 2012

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