14q11 abnormality and trisomy 8q are not common in Japanese T-cell prolymphocytic leukemia

Int J Hematol. 1998 Oct;68(3):291-6. doi: 10.1016/s0925-5710(98)00074-7.

Abstract

We studied ten cases of Japanese T-cell prolymphocytic leukemia (T-PLL) collected over the last 9 years. Median age was 61 years with a male predominance (M:F, 8:2). The main disease features were splenomegaly, lymphadenopathy, hepatomegaly, skin lesions and serous effusions. The clinical course was progressive with a median survival of 10 months. Immunophenotyping showed that the prolymphocytes had a post-thymic phenotype (TdT-, CD1a-, CD2+, CD3+, CD5+, CD7+) with a predominant CD4+ immunophenotype. Cytogenetic analysis showed no consistent abnormalities. 14q abnormality and trisomy 8q, which are frequently seen in T-PLL of Western countries, were found in only two and zero cases, respectively. We conclude that the clinical and biological characteristics of T-PLL in Japan are almost the same as those in Western countries. However, the cytogenetic findings of T-PLL in Japan might be different.

Publication types

  • Clinical Trial
  • Controlled Clinical Trial

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Chromosome Aberrations / genetics*
  • Chromosome Disorders
  • Chromosomes, Human, Pair 14*
  • Chromosomes, Human, Pair 8*
  • Female
  • Humans
  • Japan
  • Leukemia, Prolymphocytic / genetics*
  • Leukemia, T-Cell / genetics*
  • Male
  • Middle Aged
  • Trisomy*