Abstract:
OBJECTIVE:Myelodysplastic syndrome (MDS) is recognized as a preleukemic disorder with a variable risk of transformation to acute myeloid leukemia. Usually the blast cells in leukemia are transformed after MDS displays a myeloid phenotype. Lymphoid progression had been reported as myeloid-lymphoid hybrid or early B phenotype, but our patient transformed acute T-lymphoblastic leukemia, which is a rare lymphoid transformation. CLINICAL PRESENTATION AND INTERVENTION:We present a case of refractory anemia with excess of blast that transformed into acute T-cell lymphoblastic leukemia. MDS was diagnosed in a 69-year-old man in April 2007. Twelve month later, he developed T-acute lymphoblastic leukemia. The blasts were positive for expression of CD2, CD3, CD5, CD7, CD45, and HLA-DR, leading to a diagnosis of T-lymphoblastic leukemia. The patient was treated with chemotherapy, but he died of multiple organ failure. CONCLUSION:The mechanism of lymphoid transformation is not yet fully understood. This case clinically supports the nature of MDS as a pluripotent hematopoietic stem cell disorder. MDS often transforms into acute leukemia, usually of a myeloid phenotype. The transformation of MDS into acute lymphoblastic leukemia is extremely rare.
journal_name
J Natl Med Assocjournal_title
Journal of the National Medical Associationauthors
Serefhanoglu S,Goker H,Buyukasik Y,Sayinalp N,Ozcebe OIdoi
10.1016/s0027-9684(15)30887-7subject
Has Abstractpub_date
2009-04-01 00:00:00pages
370-2issue
4eissn
0027-9684issn
1943-4693pii
S0027-9684(15)30887-7journal_volume
101pub_type
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journal_title:Journal of the National Medical Association
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journal_title:Journal of the National Medical Association
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