Cytogenetic study of acute lymphoblastic leukemia and its correlation with immunophenotype and genotype

1992 ◽  
Vol 59 (2) ◽  
pp. 191-198 ◽  
Author(s):  
Hwei-Fang Tien ◽  
Chiu-Hwa Wang ◽  
Fen-Yu Lee ◽  
Ming-Chi Liu ◽  
Sou-Ming Chuang ◽  
...  
JMS SKIMS ◽  
2020 ◽  
Vol 23 (2) ◽  
Author(s):  
Faisal R Guru ◽  
Nisar Ahmad Syed ◽  
Shumail Bashir ◽  
Sanudev Sadanandan Vp ◽  
Hashim Kunju Ismail ◽  
...  

Background The complete cytogenetic and immunophenotyping data in children suffering from acute lymphoblastic leukemia (ALL) in Jammu and Kashmir is scarce. To bridge this knowledge gap the present study proposes to evaluate the immunophenotype and cytogenetic profile of pediatric ALL patients treated in our hospital. Material and methods This hospital-based observational study was conducted on 180 pediatric patients aged between 1  to 18 years who had visited the Paediatric unit of the  Department of Medical Oncology at Sher-I -Kashmir Institute of Medical Science, Srinagar ,Jammu and Kashmir between the January 2015 to December 2019. Result Among the study participants, 57.8% were male and 42.2% were female with a mean age of 9.24 years and median of 8 Years. Among the participants, 57.2% were below 10 years of age and 42.8% were above 10years of age. CNS disease was reported in 7.8%  of the study participants.  63.3% patients  had a TLC count of less than 20000. Immunophenotyping data revealed pre-B ALL in 77.8% of children. Cytogenetic study was conducted on 153 patients among them 74.4% had a normal karyotype, 7.2% s had hyperdiploidy and 3.3% had hypodiploidy. The FISH analysis showed that 23.3% of study participants were positive for the TEL-AML study, 11.1% were positive for BCR-ABL analysis and 4.4% of participants were positive for MLL gene analysis. The overall survival in the study population was 78.9% among the study participants. Only the MLL gene rearrangement analysis showed a statistically significant correlation with the survival analysis (P<0.5). Conclusion In summary, the present study reported the complete cytogenetic and immunophenotyping profile of the children suffering from acute lymphoblastic leukemia in Jammu and Kashmir.


2010 ◽  
Vol 5 (2) ◽  
pp. 179-183 ◽  
Author(s):  
George A. Alexiou ◽  
Maria Moschovi ◽  
George Georgoulis ◽  
Rosalia Neroutsou ◽  
Kalliopi Stefanaki ◽  
...  

Radiation-induced brain tumors are suggested to be the late complication of acute lymphoblastic leukemia (ALL) treatment. High-grade gliomas, meningiomas, and sarcomas are the most frequent neoplasms. Secondary anaplastic oligodendrogliomas are exceedingly rare. Five cases of pure anaplastic oligodendroglioma have been reported in the literature, and only 1 case was in a child after ALL treatment. The authors present 2 cases of pediatric anaplastic oligodendroglioma after treatment of ALL. Furthermore, they performed a molecular cytogenetic study and found loss of 1p in both cases. The authors provide a review of the previous cases and discuss their findings.


1984 ◽  
Vol 18 (2) ◽  
pp. 215-221 ◽  
Author(s):  
Christiane Werner-Favre ◽  
Marinette Wyss ◽  
Christine Cabrol ◽  
Françoise Félix ◽  
Rita Guenin ◽  
...  

1994 ◽  
Vol 23 (5) ◽  
pp. 413-421 ◽  
Author(s):  
Angelika Berger ◽  
Sabine Strehl ◽  
Andreas Hekele ◽  
Peter F. Ambros ◽  
Oskar A. Haas ◽  
...  

Blood ◽  
2010 ◽  
Vol 115 (2) ◽  
pp. 206-214 ◽  
Author(s):  
Anthony V. Moorman ◽  
Lucy Chilton ◽  
Jennifer Wilkinson ◽  
Hannah M. Ensor ◽  
Nick Bown ◽  
...  

AbstractChromosomal abnormalities are increasingly used to risk stratify adults with acute lymphoblastic leukemia. Published data describing the age-specific incidence of chromosomal abnormalities and their prognostic relevance are largely derived from clinical trials. Trials frequently have age restrictions and low recruitment rates. Thus we investigated these factors in a population-based cohort of 349 patients diagnosed during the course of 19 years in the northern part of England. The incidence of most chromosomal abnormalities varied significantly with age. The incidence of t(9;22)(q34;q11) increased in each successive decade, up to 24% among 40- to 49-year-old subjects. Thereafter the incidence reached a plateau. t(4;11)(q21;q23) and t(1;19)(q23;p13) were a rare occurrence among patients older than 60 years of age. In contrast, the frequency of t(8;14)(q24;q32) and t(14;18)(q32;q21) increased with age. High hyperdiploidy occurred in 13% of patients younger than 20 years of age but in only 5% of older patients. The incidence of low hypodiploidy/near-triploidy and complex karyotype increased with age from 4% (15-29 years) to 16% (≥ 60 years). Overall survival varied significantly by age and cytogenetics. Older patients and those with t(9;22), t(4;11), low hypodiploidy/near-triploidy, or complex karyotype had a significantly inferior outcome. These population-based results demonstrate the cytogenetic heterogeneity of adult acute lymphoblastic leukemia. These data will inform the delivery of routine clinical services and the design of new age-focused clinical trials.


2005 ◽  
Vol 156 (1) ◽  
pp. 54-58 ◽  
Author(s):  
Giorgina Specchia ◽  
Francesco Albano ◽  
Luisa Anelli ◽  
Antonella Zagaria ◽  
Arcangelo Liso ◽  
...  

1990 ◽  
Vol 10 (1) ◽  
pp. 31-36
Author(s):  
Chen Zhong ◽  
Yang Ai-de ◽  
Fei Hong-ao ◽  
Gong Wei-long

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