Cytogenetic studies of Acute Myeloid Leukemia | ||
| The Egyptian Journal of Hospital Medicine | ||
| Article 12, Volume 38, Issue 1, January 2010, Pages 131-139 PDF (363.86 K) | ||
| Document Type: Original Article | ||
| DOI: 10.21608/ejhm.2010.17378 | ||
| Author | ||
| Tarek Abd -Alla Atia | ||
| Histology Dept. Faculty of Medicine, Al-Azhar University, Cairo | ||
| Abstract | ||
| characterized by expansion of undifferentiated myeloid progenitors. Acquired chromosomal anomaly particularly reciprocal translocations constitute one of the major events contribute to leukemogenesis. Patient and Methods: 45 untreated, newly diagnosed patients with de novo AML were enrolled in the present study and subjected to cytogenetic analysis. Four ml of heparinized peripheral blood were collected for 72 hours synchronized culture, and then chromosome G- banding analysis was performed using standard methods. The karyotypes were designated according to the International System for Human Cytogenetic Nomenclature (ISCN). The collected data were analyzed statistically. Result: Cytogenetic analysis and karyotype results were obtained in 45 patients with de novo AML. Males constituted 33.3%, and femalesconstituted66.7% of this group. The patients' age ranged from 17-60 years. Chromosomal anomalies have been detected in 21 out of 45 patients (46.7%). However five different types of chromosome anomalies have been detected; where seven cases (33.3%) carrying t(15;17)( q22;q21); six cases (28.5%) carrying t(8;21)(q22;q22); three cases (14.3%) had trisomy 8; three cases (14.3%) had monosomy 7; and lastly two cases (9.5%) carrying inv(3)(q21q26). Conclusion: Conventional cytogenetic analysis reliability detects chromosomal abnormalities in AML patients at the time of diagnosis. Chromosomal anomalies detected in Egyptian AML patients, are similar to some extent to those recorded in other areas of the world. | ||
| Keywords | ||
| Cytogenetic; Myeloid Leukemia; karyotypes; trisomy; monosomy | ||
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