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pubmed-article:3374171pubmed:abstractTextWe report a patient with acute eosinophilic leukemia and a translocation (10;11)(p14;q21). Clinically, the disease was characterized by extreme hypereosinophilia with most eosinophils being immature, pronounced marrow infiltration with abnormal eosinophil precursors, skin and lymphoid infiltration with leukemic eosinophils, and only a brief remission from chemotherapy. This is the second report of a patient with this cytogenetic/clinicopathological association. In our patient, t(10;11)(p14;q21) was the sole karyotypic abnormality seen in the bone marrow, both at diagnosis and relapse. Thus, acute eosinophilic leukemia with t(10;11)(p14;q21) appears to be a rare, new clinical/cytogenetic association. Because both patients with this translocation responded only briefly to chemotherapy, this chromosomal abnormality may confer a poor prognosis.lld:pubmed
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pubmed-article:3374171pubmed:authorpubmed-author:SchifferC ACAlld:pubmed
pubmed-article:3374171pubmed:authorpubmed-author:TestaJ RJRlld:pubmed
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pubmed-article:3374171pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:3374171pubmed:year1988lld:pubmed
pubmed-article:3374171pubmed:articleTitleAcute eosinophilic leukemia with a (10;11) chromosomal translocation.lld:pubmed
pubmed-article:3374171pubmed:affiliationUniversity of Maryland Cancer Center, Baltimore.lld:pubmed
pubmed-article:3374171pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:3374171pubmed:publicationTypeResearch Support, U.S. Gov't, Non-P.H.S.lld:pubmed
pubmed-article:3374171pubmed:publicationTypeCase Reportslld:pubmed
pubmed-article:3374171pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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