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Case Reports
. 2014 Sep;30(Suppl 1):186-9.
doi: 10.1007/s12288-013-0322-8. Epub 2014 Jan 23.

A Case of AML-M2 with Sole Interstitial Deletion in 9q Without AML1-ETO/Inv 16 Rearrangement and FLT3/NPMI Mutations

Affiliations
Case Reports

A Case of AML-M2 with Sole Interstitial Deletion in 9q Without AML1-ETO/Inv 16 Rearrangement and FLT3/NPMI Mutations

G Sandhya Devi et al. Indian J Hematol Blood Transfus. 2014 Sep.

Abstract

Conventional/molecular cytogenetics is important in identification of genomic abnormalities, for prognostication and in risk stratification of de novo patients with acute myeloid leukemias (AML). Here we present an AML M2 case showing the sole karyotypic abnormality, the rare interstitial deletion in the long arm of chromosome 9 with the loss of segment q12-q13.

Keywords: AML-M2; CD7; Conventional cytogenetics; Del 9q.

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Figures

Fig. 1
Fig. 1
Peripheral smear of an AML-M2 case showing blasts with Auer rods (Leishman stain, oil immersion X100)
Fig. 2
Fig. 2
The gated population of neoplastic cells showing positivity for CD13, CD33, CD34, CD45, CD117, HLA DR, with aberrant expression of CD7
Fig. 3
Fig. 3
Karyotype shows the abnormality—46,XY,del(9)(q12 q13)

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