Skip to main navigation Skip to search Skip to main content

Myelodysplastic syndrome with isolated deletion of chromosome 20q: An indolent disease with minimal morphological dysplasia and frequent thrombocytopenic presentation

  • Raavi Gupta
  • , Chad P. Soupir
  • , Vandita Johari
  • , Robert P. Hasserjian

Research output: Contribution to journalArticlepeer-review

59 Scopus citations

Abstract

The present study analysed the clinicopathological features of nine myelodysplastic syndrome (MDS) patients in which del(20q) was the sole cytogenetic abnormality and a control group of 17 adult patients with idiopathic thrombocytopenic purpura (ITP). Seven of nine del(20q) patients were thrombocytopenic and six of nine were mildly anaemic at presentation. There was no significant morphological dysplasia identified in the del(20q) group as compared with the ITP group. These results indicate that MDS with del(20q) commonly presents with thrombocytopenia and has minimal morphological dysplasia. Cytogenetic analysis on adult patients undergoing bone marrow sampling for thrombocytopenia may help avoid misdiagnosis of MDS with del(20q) as ITP.

Original languageEnglish
Pages (from-to)265-268
Number of pages4
JournalBritish Journal of Haematology
Volume139
Issue number2
DOIs
StatePublished - Oct 2007

Keywords

  • Cytogenetics
  • Histopathology
  • Idiopathic thrombocytopenic purpura
  • Myelodysplastic syndromes
  • Thrombocytopenia

Fingerprint

Dive into the research topics of 'Myelodysplastic syndrome with isolated deletion of chromosome 20q: An indolent disease with minimal morphological dysplasia and frequent thrombocytopenic presentation'. Together they form a unique fingerprint.

Cite this