| Literature DB >> 26622430 |
Hongzai Guan1, Jing Liu2, Xiaofang Guo1, Chunmei Wu1, Huawei Yu3.
Abstract
Acute promyelocytic leukemia (APL) with variant translocations is rare. The patient of the present case report, a 2-year-old male with a microgranular variant of APL carrying der(17) ins(17;15) translocation, exhibited fever and epistaxis. The complete blood count showed marked leukocytosis with 72% atypical promyelocytes, anemia and thrombocytopenia. Conventional cytogenetic analysis of the bone marrow cells revealed a karyotype of 47, XY, add(3)(q29), -7, ins(17;15)(q12;q14q22),+21,+mar. The promyelocytic leukemia/retinoic acid receptor α (PML/RARα) rearrangement and insertion were confirmed by fluorescence in situ hybridization. The PML/RARα transcripts were not detected by the reverse transcription polymerase chain reaction, and the patient was diagnosed with microgranular variant M3 APL. The patient achieved remission after a 30-day treatment and was still in remission during a recent follow-up. The present findings suggest that the ins(17;15) variant in APL may not be associated with an unfavorable prognosis. In summary, we reported an extremely rare case of APL with der(17) ins(17;15) abnormality in a pediatric patient and reviewed the literature.Entities:
Keywords: acute promyelocytic leukemia; chromosomal aberrations; fluorescence in situ hybridization; ins(17;15)(q12;q14q22); microgranular acute promyelocytic leukemia; prognosis
Year: 2015 PMID: 26622430 PMCID: PMC4533157 DOI: 10.3892/etm.2015.2583
Source DB: PubMed Journal: Exp Ther Med ISSN: 1792-0981 Impact factor: 2.447