| Literature DB >> 15474155 |
Meera B Chitlur1, Kanta Bhambhani, Anwar N Mohamed, Yaddanapudi Ravindranath, Süreyya Savaşan.
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).Entities:
Mesh:
Year: 2004 PMID: 15474155 DOI: 10.1016/j.cancergencyto.2004.02.019
Source DB: PubMed Journal: Cancer Genet Cytogenet ISSN: 0165-4608