Complex Karyotype in Hematological Diseases: A 6-Year Single Centre Study from Pakistan

Background. Most of the hematological disorders are heterogenous with regard to morphology, immunophenotype, and genetic rearrangements. Multiple recurrent chromosomal aberrations have been identified by conventional cytogenetic analysis, which is now widely recognized as one of the most important d...

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Main Authors: Samra Waheed, Jawad Hassan, Maliha Naz, Sidra Maqsood, Madiha Abid, Saira Shan, Muhammad Nadeem, Tahir S. Shamsi
Format: Article
Language:English
Published: Hindawi Limited 2018-01-01
Series:Journal of Oncology
Online Access:http://dx.doi.org/10.1155/2018/2019239
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spelling doaj-e7e6977680bf44e2ba27751cf94bf5eb2020-11-24T21:05:37ZengHindawi LimitedJournal of Oncology1687-84501687-84692018-01-01201810.1155/2018/20192392019239Complex Karyotype in Hematological Diseases: A 6-Year Single Centre Study from PakistanSamra Waheed0Jawad Hassan1Maliha Naz2Sidra Maqsood3Madiha Abid4Saira Shan5Muhammad Nadeem6Tahir S. Shamsi7National Institute of Blood Disease and Bone Marrow Transplantation, Karachi, PakistanNational Institute of Blood Disease and Bone Marrow Transplantation, Karachi, PakistanNational Institute of Blood Disease and Bone Marrow Transplantation, Karachi, PakistanNational Institute of Blood Disease and Bone Marrow Transplantation, Karachi, PakistanNational Institute of Blood Disease and Bone Marrow Transplantation, Karachi, PakistanNational Institute of Blood Disease and Bone Marrow Transplantation, Karachi, PakistanNational Institute of Blood Disease and Bone Marrow Transplantation, Karachi, PakistanNational Institute of Blood Disease and Bone Marrow Transplantation, Karachi, PakistanBackground. Most of the hematological disorders are heterogenous with regard to morphology, immunophenotype, and genetic rearrangements. Multiple recurrent chromosomal aberrations have been identified by conventional cytogenetic analysis, which is now widely recognized as one of the most important diagnostic and prognostic determinants in these patients. Though rarer, complex karyotype has been associated with worst prognosis. Materials and Methods. A total of 1185 bone marrow or peripheral blood cytogenetics samples were taken with different hematological diseases. They included both benign and malignant disease entities. In each case, cells were cultured and conventional cytogenetic analysis was performed. Results. Among 1185 subjects, 41 (3.4%) patients possessed complex cytogenetic abnormalities. Out of these 41, 33 (80%) were males. The mean age was 37 years (median age 39 years). Myelodysplastic syndromes had the most numbers of complex karyotypes (8%), followed by acute myeloid leukemia (7%) and acute lymphoblastic leukemia (4%). Also we found few patients with acute promyelocytic leukemia, aplastic anemia , chronic myeloid leukemia, and diffuse large B cell Lymphoma possessing complex karyotype. Frequencies of different cytogenetic abnormalities were assessed with respect to disease as well as independently. Trisomy 21 was the most common chromosomal abnormality found in 28% of patients. Conclusion. Complex karyotype was most frequently associated with myelodysplastic syndromes and acute myeloid leukemia. Trisomy 21 and deletion 5q were the commonest cytogenetic abnormalities found. We also assessed complex karyotype in benign diseases and detected one patient of aplastic anemia with complex karyotype. This is the first study highlighting the presence of complex karyotypes in hematological disorders in our region.http://dx.doi.org/10.1155/2018/2019239
collection DOAJ
language English
format Article
sources DOAJ
author Samra Waheed
Jawad Hassan
Maliha Naz
Sidra Maqsood
Madiha Abid
Saira Shan
Muhammad Nadeem
Tahir S. Shamsi
spellingShingle Samra Waheed
Jawad Hassan
Maliha Naz
Sidra Maqsood
Madiha Abid
Saira Shan
Muhammad Nadeem
Tahir S. Shamsi
Complex Karyotype in Hematological Diseases: A 6-Year Single Centre Study from Pakistan
Journal of Oncology
author_facet Samra Waheed
Jawad Hassan
Maliha Naz
Sidra Maqsood
Madiha Abid
Saira Shan
Muhammad Nadeem
Tahir S. Shamsi
author_sort Samra Waheed
title Complex Karyotype in Hematological Diseases: A 6-Year Single Centre Study from Pakistan
title_short Complex Karyotype in Hematological Diseases: A 6-Year Single Centre Study from Pakistan
title_full Complex Karyotype in Hematological Diseases: A 6-Year Single Centre Study from Pakistan
title_fullStr Complex Karyotype in Hematological Diseases: A 6-Year Single Centre Study from Pakistan
title_full_unstemmed Complex Karyotype in Hematological Diseases: A 6-Year Single Centre Study from Pakistan
title_sort complex karyotype in hematological diseases: a 6-year single centre study from pakistan
publisher Hindawi Limited
series Journal of Oncology
issn 1687-8450
1687-8469
publishDate 2018-01-01
description Background. Most of the hematological disorders are heterogenous with regard to morphology, immunophenotype, and genetic rearrangements. Multiple recurrent chromosomal aberrations have been identified by conventional cytogenetic analysis, which is now widely recognized as one of the most important diagnostic and prognostic determinants in these patients. Though rarer, complex karyotype has been associated with worst prognosis. Materials and Methods. A total of 1185 bone marrow or peripheral blood cytogenetics samples were taken with different hematological diseases. They included both benign and malignant disease entities. In each case, cells were cultured and conventional cytogenetic analysis was performed. Results. Among 1185 subjects, 41 (3.4%) patients possessed complex cytogenetic abnormalities. Out of these 41, 33 (80%) were males. The mean age was 37 years (median age 39 years). Myelodysplastic syndromes had the most numbers of complex karyotypes (8%), followed by acute myeloid leukemia (7%) and acute lymphoblastic leukemia (4%). Also we found few patients with acute promyelocytic leukemia, aplastic anemia , chronic myeloid leukemia, and diffuse large B cell Lymphoma possessing complex karyotype. Frequencies of different cytogenetic abnormalities were assessed with respect to disease as well as independently. Trisomy 21 was the most common chromosomal abnormality found in 28% of patients. Conclusion. Complex karyotype was most frequently associated with myelodysplastic syndromes and acute myeloid leukemia. Trisomy 21 and deletion 5q were the commonest cytogenetic abnormalities found. We also assessed complex karyotype in benign diseases and detected one patient of aplastic anemia with complex karyotype. This is the first study highlighting the presence of complex karyotypes in hematological disorders in our region.
url http://dx.doi.org/10.1155/2018/2019239
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