Literature DB >> 1581883

Monosomy 20 in childhood acute lymphoblastic leukemia.

M Silengo1, E Vassallo, E Barisone, R Miniero, E Madon.   

Abstract

We report two cases of acute lymphoblastic leukemia (ALL) with loss of chromosome 20 as the only karyotypic abnormality detected in the blast cells. The first patient is a 12-year-old boy studied at diagnosis. He represents the only case of monosomy 20 in our series of 90 pediatric ALL successfully karyotyped at diagnosis. In the second patient, monosomy 20 was detected at the second hematologic relapse, 12 years after the initial diagnosis; cytogenetic studies were not performed at disease onset.

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Year:  1992        PMID: 1581883     DOI: 10.1016/0165-4608(92)90212-q

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


  1 in total

1.  An acquired stable variant of a dicentric dic(9;20) and complex karyotype in a Syrian childhood B-acute lymphoblastic leukemia case.

Authors:  Abdulsamad Wafa; Rami A Jarjour; Abdulmunim Aljapawe; Suher ALmedania; Thomas Liehr; Joana B Melo; Isabel M Carreira; Moneeb A K Othman; Walid Al-Achkar
Journal:  Mol Cytogenet       Date:  2020-07-10       Impact factor: 2.009

  1 in total

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