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CASE REPORTS in HAEMATOLOGY
(Paper co-edited with the European LeukemiaNet)
Translocation (X;20)(q13;q13.3): a nonrandom abnormality in four patients with myeloid disorders: case 2
WARNING: on Feb 2008, we have been aware that this case had simultaneously been published in another Journal (namely Cancer Genet Cytogenet), although double reports are objectionable.
Kavita S Reddy, Kathy Richkind
 
Clinics
Age and sex : 61 year(s) old female patient.
Organomegaly : no hepatomegaly ; no splenomegaly ; no enlarged lymph nodes ; no central nervous system involvement
Blood
WBC : 3.05 x 109/l; Hb : 8.1 g/dl; platelets : 62 x 109/l;
Cyto pathology classification
Precise diagnosis : Myelofibrosis -> acute leukemia
Survival
Treatment : Induction treatment: topotecan and cytarabine
Relapse : -
Status : Alive
Survival : 55 month(s)
Karyotype
Sample : PB ; culture time : 24/48 h, unstimulated cultures ; banding : G-banding
Results : 46,X,t(X;20)(q13;q13.3),der(1;7)(q10;p10)[20]/46,XX[1]
Fig. 1. Partial karyotypes of the translocation t(X;20)(q13;q13.3) for cases 1•4 (top to bottom). Arrows indicate the derivatives 20 and X.
Internal links
Atlas Cardt(X;20)(q13;q13)
Case ReportTranslocation (X;20)(q13;q13.3): a nonrandom abnormality in four patients with myeloid disorders: case 1
Case ReportTranslocation (X;20)(q13;q13.3): a nonrandom abnormality in four patients with myeloid disorders: case 3
Case ReportTranslocation (X;20)(q13;q13.3): a nonrandom abnormality in four patients with myeloid disorders: case 4
Bibliography
Characterization by chromosome painting of balanced and unbalanced X chromosome translocations in myelodysplastic syndromes.
Michaux L, Wlodarska I, Mecucci C, Hernandez JM, Van Orshoven A, Michaux JL, Van den Berghe H.
Cancer Genet Cytogenet 1995; 82: 17•22.
PMID 7627929
 
Translocation (X;20)(q13.1;q13.3) as a primary chromosomal finding in two patients with myelocytic disorders.
Gray BA, Cornfield D, Bent-Williams A, Zori RT.
Cancer Genet Cytogenet 2003; 141: 169•174.
PMID 12606138
 
Translocation (X;20)(q13;q13.3): a nonrandom abnormality in four patients with myeloid disorders.
Reddy KS, Richkind K, Ross M, Seirra R.
Cancer Genet Cytogenet 2005; 151: 70-73.
PMID 15676151
 

Contributor(s)
Written01-2005Kavita S Reddy, Kathy Richkind
Citation
This paper should be referenced as such :
Reddy KS, Richkind KE . Translocation (X;20)(q13;q13.3): a nonrandom abnormality in four patients with myeloid disorders: case 2. Atlas Genet Cytogenet Oncol Haematol. January 2005 .
URL : http://AtlasGeneticsOncology.org/Reports/0X20ReddyID100010.html

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indexed on : Thu Apr 17 14:15:25 2008


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