Title of article
Acute megakaryoblastic leukemia with t(17;22)(q21;q13) and liver dysfunction
Author/Authors
Chitlur، نويسنده , , Meera B. and Bhambhani، نويسنده , , Kanta and Mohamed، نويسنده , , Anwar N. and Ravindranath، نويسنده , , Yaddanapudi and Sava?an، نويسنده , , Süreyya، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2004
Pages
2
From page
167
To page
168
Abstract
The t(1;22)(p13;q13) is associated with acute megakaryoblastic leukemia (AMKL) seen mostly in young infants and known to have a poor prognosis. A 5-year-old child had prolonged prothrombin and partial thromboplastin times, low albumin, and decreased vitamin K-dependent coagulation factors and factor V activities at the time of AMKL diagnosis. All of these factors normalized following chemotherapy when remission was achieved. Cytogenetic analysis revealed a female karyotype with a balanced t(17;22)(q21;q13). Here, we present an AMKL pediatric case with a novel translocation and significant hepatocellular dysfunction that resolved with chemotherapy. The t(17;22) (q21;q13) may represent a variant of t(1;22)(p13;q13).
Journal title
Cancer Genetics and Cytogenetics
Serial Year
2004
Journal title
Cancer Genetics and Cytogenetics
Record number
1826324
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