[Home ] [Archive]   [ فارسی ]  
:: Main :: About us :: Current Issue :: Archive :: Search :: Submit :: Contact ::
Main Menu
Home::
Journal Information::
Articles archive::
For Authors::
For Reviewers::
Subscription::
News& Events::
Contact us::
Site Facilities::
Ethics & Permissions::
::
Search in website

Advanced Search
..
Receive site information
Enter your Email in the following box to receive the site news and information.
..
Indexing
                        
..
:: Volume 14, Issue 2 (Summer 2017) ::
Sci J Iran Blood Transfus Organ 2017, 14(2): 118-125 Back to browse issues page
Frequency of Chromosome Disorders in the Childrenwith Acute Leukemia Referred to the OncSanandaj Besat Hospitalology Ward of
B. Moradveisi , H. Safari , D. Roshani , B. Khalafi , R. Raghizadeh Sarvestani
Keywords: Key words: Leukemia, Chromosome Disorders, Children
Full-Text [PDF 1400 kb]   (1375 Downloads)     |   Abstract (HTML)  (4325 Views)
Type of Study: Research | Subject: Hematology and Oncology
Published: 2017/06/18
Full-Text:   (3846 Views)
References :  
  1. International incidence of childhood cancer, Vol.II. IARC Sci Publ 1998; 2(144): 1-391.
  2. Belson M, Kingsley B, Holmes A. Risk factors for acute leukemia in children: a review. Environ Health Perspect 2007; 115(1): 138-45.
  3. Onciu M, Pui CH. Diagnosis and classification. In: Pui Ching-Hon. Childhood Leukemias. New York: Cambridge University Press; 2006. p. 21-47.
  4. Abbasnejad M, Shayanfar N, Kadivar M, Taraz Jamshidi Sh, Naeimi T, Gharib A. [Robbins Basic Pathology]. 9th ed. Tehran: Andishe-Rafi; 2007. P. 668.
  5. Kavehmanesh Z. [Nelson Textbook of Pediatrics]. Tehran: Abasaleh Publications; 2004. p. 1456.
  6. Grimwade D, Walker H, Oliver F, Wheatley K, Harrison C, Harrison G, et al. The importance of diagnostic cytogenetics on outcome in AML: Analysis of1,612 patients entered into the MRC AML 10 trial. The Medical Research Council Adult and Children’s Leukaemia Working parties. Blood 1998; 92(7): 2322-33.
  7. Wiemels J. Chromosomal translocations in childhood leukemia: naturalhistory, mechanisms, and epidemiology. J Natl Cancer Inst Monogr 2008; 39(51): 87-90.
  8. Liu PP, Tarle SA, Hajra A, Claxton DF, Marlton P, Freedman M, et al. Fusion between transcription factor CBF beta/PEBP2 beta and a myosin heavy chain in acute myeloid leukemia. Science 1993; 261(5124): 1041-4.
  9. De The H, Chomienne C, Lanotte M, Degos L, Dejean A. The t(15;17) translocation of acute promyelocytic leukaemia fuses the retinoic acid receptor alpha gene to a novel transcribed locus. Nature  1990; 347(6293): 558-61.
  10. Grimwade D. The pathogenesis of acute promyelocytic leukaemia: evaluation of the role of molecular diagnosis and monitoring in the management of the disease. Br J Haematol 1999; 106(3): 591-613.
  11. Greaves M. Childhood leukaemia. BMJ 2002; 324(7332): 283-7.
  12. McHale CM, Wiemels JL, Zhang L, Ma X, Buffler PA, Guo W, et al. Prenatal origin of TEL-AML1-positive acute lymphoblastic leukemia in children born in
California. Genes Chromosomes Cancer 2003; 37(1): 36-43.
  1. Wiemels JL, Xiao Z, Buffler PA, Maia AT, Ma X, Dicks BM, et al.  In utero origin of t(8;21) AML1-ETO translocations in childhood acute myeloid leukemia. Blood 2002; 99(10): 3801-5.
  2. Patte C, Michon J, Frappaz D, Leverger G, Rubie H, Soussain C, et al. Therapy of Burkitt andother B-cell acute tymphoblastic leukaemia and lymphoma: experience with the LMB protocols of the SFOP (French Paediatric Oncology Society) in children and adults. Baillieres Clin Haematol 1994; 7(2): 339-48.
  3.  Williams DL, Look AT, Melvin SL, Roberson PK, Dahl G, Flake T, et al. New chromosomal translocations correlate with specific lmmunophenotypes of childhood acute lymphoblastic leukemia. Cell 1984; 36(1): 101-9.
  4. Marques EA, Neves L, Fonseca TC, Lins  MM, Pedrosa F, Lucena-Silva N. Molecular Findings in Childhood Leukemia in Brazil: High Frequency of MLL-ENL Fusion/t(11;19) in Infant Leukemia. J Pediatr Hematol Oncol 2011; 33(6): 470-4.
  5. Soszynska K, Mucha B, Debski R, Skonieezka K, Duszenko E, Koltan A, et al. The application of conventional cytogenetics, FISH, and RT-PCR to detect genetic changes in 70 children with ALL. Ann Hematol 2008; 87(12): 991-1002.
  6. Raimondi SC, Chang MN, Ravindranath Y, Behm FG, Gresik MV, Steuber CP, et al. Chromosomal abnormalities in 478 children with acute myeloid leukemia: clinical characteristics and treatment outcome in a cooperative oncology pediatric group study-POG 8821. Blood 1999; 94(11): 3707-16.
  7. Nazari Sh, Shafiei A, Abdollah Gorji F. Cytogenetic study of prognostic determinants in children with acute lymphoblastic leukemia. Sci J Iran Blood Transfus Organ 2008; 5(2): 117-23. [Article in Farsi]
  8. Al-Kzayer LFSakashita KMatsuda KAl-Hadad SAAl-Jadiry MFAbed WMet al. Genetic evaluation of childhood acute lymphoblastic leukemia in Iraq using FTA cards. Pediatr Blood Cancer 2012; 59(3): 461-7.
 
 
 
 
 
 
 
 
 
 
 


 
Original  Article
 

 
 
 
Sci J Iran Blood Transfus Organ 2017; 14(2): 118-125
Frequency of Chromosome Disorders in the Children
with Acute Leukemia Referred to the Oncology Ward of Sanandaj Besat Hospital
 
Moradveisi B.1, Safari H.2, Roshani D.1, Khalafi B.2, Taghizadeh Sarvestani R.3
 
 
1Faculty of Medicine, Kurdistan University of Medical Sciences, Sanandaj, Iran
2Student Research Committee, Kurdistan University of Medical Sciences, Sanandaj, Iran
3Faculty of Medicine, Shahroud University of Medical Sciences, Shahroud, Iran 
 
 
Abstract
Background and Objectives
Blood Malignancies are the most frequent cancers in children including about 45% of diagnosed cancers in children. Chromosome disorders are found in most of patients with acute lymphoblastic leukemia. These disorders present valuable information for prognostic determinants.
 
Materials and Methods
This descriptive study includes all the children with acute leukemia having referred to the oncology ward of Besat Hospital of Sanandaj from 1385 to the end of the first half of 1394. Peripheral blood smear and bone marrow aspirations were taken from the children; RT-PCR method was used for determination of chromosome karyotypes so as to detect chromosome disorders. The data were analyzed by SPSS 11.5 & c2 test.
Results
Among 75 cases, 12 chromosome genotypes were observed. Normal chromosome genotype has the highest frequency with 41 cases (54.7%). t(12-21) chromosome disorder observed in 15 cases (20%) was the most frequent disorder. t(15-17) chromosome disorder observed in 5 cases (6.5%) was the next most frequent disorder. The only chromosome disorder observed in T lymphocyte leukemia was 47xy + 21 with the frequency of 1 case.
 
Conclusions
Based on the research findings, 54.7% of the children have no chromosome disorders. Different results are reported in different researches. Due to the importance of finding the types of chromosome translocation for prognostic determinants in children with leukemia, more research is required.
 
Key words: Leukemia, Chromosome Disorders, Children
 
 
 
 
 
 
Received: 20  Jul  2016
Accepted: 21 Jan 2017
 
 
 

Correspondence: Taghizadeh Sarvestani R., MD. Assistant Professor of Faculty of Medicine, Shahroud University of Medical Sciences.
Postal Code: 6617967617, Shahroud, Iran. Tel: (+9823) 32385890; Fax: (+9823) 32385890
E-mail: rt_sarvestani@yahoo.com
Send email to the article author

Add your comments about this article
Your username or Email:

CAPTCHA


XML   Persian Abstract   Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Moradveisi B, Safari H, Roshani D, Khalafi B, Raghizadeh Sarvestani R. Frequency of Chromosome Disorders in the Childrenwith Acute Leukemia Referred to the OncSanandaj Besat Hospitalology Ward of . Sci J Iran Blood Transfus Organ 2017; 14 (2) :118-125
URL: http://bloodjournal.ir/article-1-1055-en.html


Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
Volume 14, Issue 2 (Summer 2017) Back to browse issues page
فصلنامه پژوهشی خون Scientific Journal of Iran Blood Transfus Organ
The Scientific Journal of Iranian Blood Transfusion Organization - Copyright 2006 by IBTO
Persian site map - English site map - Created in 0.06 seconds with 39 queries by YEKTAWEB 4645