Acute Myeloid Leukemia with Concurrent Inversion 16 and Trisomy 9: A Case Report

Author:

Aman Ambreen1,Lingappa Kavitha B.1,Sujatha Deepika G.1,Rajasab Subhan Ali1,Shantala Siddapa1

Affiliation:

1. Cytogenetics Unit, Department of Pathology, Kidwai Memorial Institute of Oncology, Bangalore, Karnataka, India

Abstract

AbstractAcute myeloid leukemia (AML) are a diverse group of hematological malignancies, each with a distinct clinical, morphological, immunophenotypic, and molecular profile. The World Health Organization (WHO) classifies AML into various subtypes based on recurrent genetic abnormalities, each of which has clinico-pathological and prognostic significance. Inversion(16)(p13q22) or t(16;16)(p13q22) is a balanced structural chromosomal abnormality associated with complete remission and a favorable response to treatment. Trisomy 9 is a numerical chromosomal abnormality with an intermediate risk and is often seen in association with other cytogenetic abnormalities. We describe a case of a 36-year-old female patient who was diagnosed as AML-M4 on peripheral smear and bone marrow evaluation. Cytogenetic studies revealed concurrent presence of inv(16) and trisomy 9. To the best of our knowledge, this is the first case in published literature with simultaneous presence of inv(16)(p13q22) and trisomy 9 in de novo AML.

Publisher

Georg Thieme Verlag KG

Subject

Pharmacology

Reference13 articles.

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2. Concurrent acute myeloid leukemia with inv(16)(p13.1q22) and chronic lymphocytic leukemia: molecular evidence of two separate diseases;C M Lu;Am J Hematol,2006

3. De novo inversion (16) acute myeloid leukemia in association with trisomy 22, deletion 7q and FLT3 (ITD) associated with complete remission;A Abdallah;Archives of Medicine,2015

4. Secondary genetic lesions in acute myeloid leukemia with inv(16) or t(16;16): a study of the German-Austrian AML study group (AMLSG);P Paschka;Blood,2013

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