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PMID: 11996797 Published · ppublish English Case Reports Journal Article

New cytogenetic variant, insertion (15;17)(q22;q12q21), in an adolescent with acute promyelocytic leukemia.

Cancer genetics and cytogenetics ·Vol. 134 ·No. 1 ·2002-04-01 ·页码 55-9

Rolston R, Weck KE, Tersak JM, Sherer ME, Cumbie K, Shekhter-Levin S

Abstract

We present the case of a 15-year-old female with acute promyelocytic leukemia and a new variant chromosome rearrangement identified as ins(15;17)(q22;q12q21) by conventional cytogenetic analysis. This finding was confirmed by fluorescence in situ hybridization using the PML-RARA DNA probe and whole chromosome paints 15 and 17. A typical PML-RARA fusion transcript consistent with a breakpoint in intron 3 of the PML gene and intron 2 of the RARA gene was identified by reverse transcription polymerase chain reaction.

MeSH 主题词
Adolescent Chromosomes, Human, Pair 15/genetics Chromosomes, Human, Pair 17/genetics Female Humans In Situ Hybridization, Fluorescence Karyotyping Leukemia, Promyelocytic, Acute/genetics,pathology Translocation, Genetic
作者与单位
共 6 位作者,点击展开单位 / ORCID
Rolston Raj
Division of Molecular Diagnostics, Department of Pathology, University of Pittsburgh, Pittsburgh, PA 15213, USA.
Weck Karen E
Tersak Jean M
Sherer Maureen E
Cumbie Kathleen
Shekhter-Levin Sofia
Article Info
Journal
Cancer genetics and cytogenetics
Abbr.
Cancer Genet Cytogenet
ISSN
0165-4608
Published
2002-04-01
页码
55-9
Language
English
Country/Region
United States
NLM ID
7909240
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