Literature DB >> 20863428

Interstitial insertion of RARα gene into PML gene in a patient with acute promyelocytic leukemia (APL) lacking the classic t(15;17).

Neta Goldschmidt1, Orly Yehuda-Gafni, Deborah Abeliovich, Elena Slyusarevsky, Deborah Rund.   

Abstract

The diagnosis of APL is based on clinical and morphological tests though the final diagnosis is at the molecular level. An accurate diagnosis is important as it mandates targeted therapy to improve survival. We report a case of APL without t(15;17) in conventional cytogenetic study and with initially negative fluorescence in situ hybridization (FISH) study on cells in interphase. Reverse transcription polymerase chain reaction (RT-PCR) for the promyelocytic/retinoic acid receptor alpha gene (PML/RARα) fusion oncogene proved the clinical diagnosis as well as FISH study on cells in metaphase. The cause was a cryptic translocation of the RARα gene into PML. We reviewed 36 additional cases of APL diagnosed in our hospital since 1992. This was the only case that failed to show t(15;17) in cytogenetics. However, three cases with t(15;17) in cytogenetics had negative RT-PCR for PML/RARα. Our case emphasizes that cytogenetics, FISH and RT-PCR studies are complementary studies for the molecular diagnosis of APL.

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Year:  2010        PMID: 20863428     DOI: 10.1179/102453310X12647083621083

Source DB:  PubMed          Journal:  Hematology        ISSN: 1024-5332            Impact factor:   2.269


  4 in total

1.  Use of whole-genome sequencing to diagnose a cryptic fusion oncogene.

Authors:  John S Welch; Peter Westervelt; Li Ding; David E Larson; Jeffery M Klco; Shashikant Kulkarni; John Wallis; Ken Chen; Jacqueline E Payton; Robert S Fulton; Joelle Veizer; Heather Schmidt; Tammi L Vickery; Sharon Heath; Mark A Watson; Michael H Tomasson; Daniel C Link; Timothy A Graubert; John F DiPersio; Elaine R Mardis; Timothy J Ley; Richard K Wilson
Journal:  JAMA       Date:  2011-04-20       Impact factor: 56.272

2.  A case of acute myeloid leukemia (AML) with an unreported combination of chromosomal abnormalities: gain of isochromosome 5p, tetrasomy 8 and unbalanced translocation der(19)t(17;19)(q23;p13).

Authors:  Christian Paar; Gabriele Herber; Daniela Voskova; Michael Fridrik; Herbert Stekel; Jörg Berg
Journal:  Mol Cytogenet       Date:  2013-09-30       Impact factor: 2.009

3.  Single-nucleotide polymorphism array-based karyotyping of acute promyelocytic leukemia.

Authors:  Inés Gómez-Seguí; Dolors Sánchez-Izquierdo; Eva Barragán; Esperanza Such; Irene Luna; María López-Pavía; Mariam Ibáñez; Eva Villamón; Carmen Alonso; Iván Martín; Marta Llop; Sandra Dolz; Oscar Fuster; Pau Montesinos; Carolina Cañigral; Blanca Boluda; Claudia Salazar; Jose Cervera; Miguel A Sanz
Journal:  PLoS One       Date:  2014-06-24       Impact factor: 3.240

4.  Acute promyelocytic leukemia with a cryptic insertion of RARA into PML on chromosome 15 due to uniparental isodisomy: A case report.

Authors:  Anna Venci; Rita Mazza; Orietta Spinelli; Luciana Di Schiena; Daniela Bettio
Journal:  Oncol Lett       Date:  2017-04-03       Impact factor: 2.967

  4 in total

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