Literature DB >> 15474155

Acute megakaryoblastic leukemia with t(17;22)(q21;q13) and liver dysfunction.

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).

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Year:  2004        PMID: 15474155     DOI: 10.1016/j.cancergencyto.2004.02.019

Source DB:  PubMed          Journal:  Cancer Genet Cytogenet        ISSN: 0165-4608


  1 in total

1.  Bi-allelic deletions within 13q14 and transient trisomy 21 with absence of GATA1s in pediatric acute megakaryoblastic leukemia.

Authors:  Stephanie A Massaro; Renu Bajaj; Farzana D Pashankar; Deborah Ornstein; Patrick G Gallagher; Diane S Krause; Peining Li
Journal:  Pediatr Blood Cancer       Date:  2011-04-29       Impact factor: 3.167

  1 in total

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