Concomitant t(8;21) and trisomy 4 in a patient with Acute Myeloid Leukemia (AML)
The t(8;21)(q22;q22) is a frequently occurring aberration in acute myeloid leukemia (AML) (18-20%) and usually correlate with French-America-British (FAB) M2 subtype. Several studies showed that patients carrying this abnormality demonstrated good response to standard chemotherapy but also have a...
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ukm-20792016-12-14T06:30:50Z http://journalarticle.ukm.my/2079/ Concomitant t(8;21) and trisomy 4 in a patient with Acute Myeloid Leukemia (AML) Phan CL, Ong TC, Chang KM, Zubaidah Z, Puteri Jamilatul NMB, The t(8;21)(q22;q22) is a frequently occurring aberration in acute myeloid leukemia (AML) (18-20%) and usually correlate with French-America-British (FAB) M2 subtype. Several studies showed that patients carrying this abnormality demonstrated good response to standard chemotherapy but also have a high incidence of disease relapse. Trisomy 4 is a rare and specific chromosomal abnormality occurring in AML M2 or M4 of the FAB subtypes. We report a case of a 33-year-old female with an apparently clinical and hematologic diagnosis of acute promyelocytic leukemia (APL) in whom cytogenetic analysis revealed an abnormal karyotype with trisomy 4, in addition to t(8;21). Trisomy 4 and t(8;21) in a patient with AML is rare. The significance of t(8;21) with trisomy 4 in AML are unclear but patients bearing this abnormality are associated with a poor prognosis. Penerbit UKM 2010 Article PeerReviewed application/pdf en http://journalarticle.ukm.my/2079/1/08MS090_4144.pdf Phan CL, and Ong TC, and Chang KM, and Zubaidah Z, and Puteri Jamilatul NMB, (2010) Concomitant t(8;21) and trisomy 4 in a patient with Acute Myeloid Leukemia (AML). Medicine & Health, 5 (1). pp. 45-48. ISSN 1823-2140 http://www.ppukm.ukm.my/ukmmcjournal/index.php |
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The t(8;21)(q22;q22) is a frequently occurring aberration in acute myeloid leukemia
(AML) (18-20%) and usually correlate with French-America-British (FAB) M2 subtype.
Several studies showed that patients carrying this abnormality demonstrated good
response to standard chemotherapy but also have a high incidence of disease relapse.
Trisomy 4 is a rare and specific chromosomal abnormality occurring in AML M2 or M4
of the FAB subtypes. We report a case of a 33-year-old female with an apparently
clinical and hematologic diagnosis of acute promyelocytic leukemia (APL) in whom
cytogenetic analysis revealed an abnormal karyotype with trisomy 4, in addition to
t(8;21). Trisomy 4 and t(8;21) in a patient with AML is rare. The significance of t(8;21)
with trisomy 4 in AML are unclear but patients bearing this abnormality are associated
with a poor prognosis. |
format |
Article |
author |
Phan CL, Ong TC, Chang KM, Zubaidah Z, Puteri Jamilatul NMB, |
spellingShingle |
Phan CL, Ong TC, Chang KM, Zubaidah Z, Puteri Jamilatul NMB, Concomitant t(8;21) and trisomy 4 in a patient with Acute Myeloid Leukemia (AML) |
author_facet |
Phan CL, Ong TC, Chang KM, Zubaidah Z, Puteri Jamilatul NMB, |
author_sort |
Phan CL, |
title |
Concomitant t(8;21) and trisomy 4 in a patient with Acute
Myeloid Leukemia (AML) |
title_short |
Concomitant t(8;21) and trisomy 4 in a patient with Acute
Myeloid Leukemia (AML) |
title_full |
Concomitant t(8;21) and trisomy 4 in a patient with Acute
Myeloid Leukemia (AML) |
title_fullStr |
Concomitant t(8;21) and trisomy 4 in a patient with Acute
Myeloid Leukemia (AML) |
title_full_unstemmed |
Concomitant t(8;21) and trisomy 4 in a patient with Acute
Myeloid Leukemia (AML) |
title_sort |
concomitant t(8;21) and trisomy 4 in a patient with acute
myeloid leukemia (aml) |
publisher |
Penerbit UKM |
publishDate |
2010 |
url |
http://journalarticle.ukm.my/2079/ http://journalarticle.ukm.my/2079/ http://journalarticle.ukm.my/2079/1/08MS090_4144.pdf |
first_indexed |
2023-09-18T19:35:09Z |
last_indexed |
2023-09-18T19:35:09Z |
_version_ |
1777405221187616768 |