Chromosomal Abnormalities in Pakistani Children with Acute Lymphoblastic Leukemia

Abstract

<b>Background:</b> Cytogenetic abnormalities have important implications in diagnosis and prognosis of acuteleukemia and are now considered an important part of the diagnostic workup at presentation. Karyotype, ifknown at the time of diagnosis, guides physicians to plan appropriate management strategies for their patients.Aim and <br/><b>Objectives</b>: To determine the cytogenetic profile of acute lymphoblastic leukemia (ALL) in Pakistanichildren in order to have insights regarding behavior of the disease. Materials and <br/><b>Methods</b>: A retrospectiveanalysis of all the cases of ALL (<15years old) diagnosed at Aga Khan University from January 2006 to June2011 was performed. Cytogenetic analysis was made for all cases using the trypsin-Giemsa banding technique.Karyotypes were interpreted using the International System for Human Cytogenetic Nomenclature (ISCN)criteria. <br/><b>Results</b>: A total of 153 patients were diagnosed as ALL during the study period, of which 127 samplessuccessfully yielded metaphase chromosomes. The male to female ratio was 1.8:1. A normal karyotype waspresent in 51.2% (n=65) of the cases whereas 48.8% (n=62) had an abnormal karyotype. Most of the abnormalcases showed hyperdiploidy(13.4%) followed by t(9;22)(q34;q11.2) (7.08%). <br/><b>Conclusions</b>: This study revealeda relative lack of good prognostic cytogenetic aberrations in Pakistani children with ALL.