Myelodysplastic syndrome with isolated deletion of chromosome 20q: an indolent disease with minimal morphological dysplasia and frequent thrombocytopenic presentation
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作者:
Gupta, Raavi
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机构:Massachusetts Gen Hosp, Dept Pathol, Boston, MA 02114 USA
Gupta, Raavi
Soupir, Chad P.
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机构:Massachusetts Gen Hosp, Dept Pathol, Boston, MA 02114 USA
Soupir, Chad P.
Johari, Vandita
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机构:Massachusetts Gen Hosp, Dept Pathol, Boston, MA 02114 USA
Johari, Vandita
Hasserjian, Robert P.
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机构:Massachusetts Gen Hosp, Dept Pathol, Boston, MA 02114 USA
Hasserjian, Robert P.
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[1] Massachusetts Gen Hosp, Dept Pathol, Boston, MA 02114 USA
[2] Columbia Univ, Med Ctr, Dept Pathol, New York, NY USA
[3] Harvard Univ, Sch Med, Boston, MA USA
[4] Baystate Med Ctr, Springfield, MA USA
[5] Tufts Univ, Sch Med, Springfield, MA 01199 USA
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.
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页码:265 / 268
页数:4
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[1]
Brunning RD, 2001, World Health Organization Classification of Tumours: Pathology and Genetics of Tumours of Haematopoietic and Lymphoid Tissues, P61