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Annals of Hematology

, Volume 98, Issue 5, pp 1319–1321 | Cite as

Coexistence of t(5;17)/NPM1-RARA and t(9;22)/BCR-ABL1 in chronic myeloid leukemia at initial diagnosis

  • Yan Li
  • Haigang Shao
  • Bin FuEmail author
Letter to the Editor
  • 65 Downloads

Dear Editor,

Additional chromosomal abnormalities (ACAs) occurs in < 10% of patients with newly diagnosed chronic myeloid leukemia (CML) in chronic phase (CP) [1, 2]. The most common ACAs are unbalanced chromosomal abnormalities, including +Ph, +8, i(17)(q10), and +19 [1, 3]. These changes are considered “major route” ACAs, whereas other infrequent aberrations are designated as “minor route” ACAs [1]. Several recurrent chromosomal rearrangements typically occurring in de novo acute myeloid leukemia (AML), such as t(8;21)(q22,q22), t(15;17)(q22;q21), and inv(16)(p13q22), have been infrequently observed as ACAs of CML (mainly the blast phase [CML-BP]) [4, 5, 6, 7, 8]. We here present a case diagnosed with CML-CP whose leukemia clone harboring both t(9;22)/BCR-ABL1 and t(5;17)/NPM1-RARA.

A 52-year-old man presented with a 2-month history of upper limb numbness. Mild splenomegaly was observed on physical examination. Laboratory tests showed leukocytosis (white blood cells, 66.27 × 10 9/L),...

Notes

Funding information

This work was supported by grants from the Hunan Provincial Science and Technology Department (CN) (2010TD2022).

Compliance with ethical standards

Informed consent

Informed consent was obtained from the patient described.

Conflict of interest

The authors declare that they have no conflict of interest.

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Copyright information

© Springer-Verlag GmbH Germany, part of Springer Nature 2018

Authors and Affiliations

  1. 1.Department of HematologyXiangya Hospital Central South UniversityChangshaPeople’s Republic of China
  2. 2.Department of HematologyThe Third Xiangya Hospital of the Central South UniversityChangshaPeople’s Republic of China

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