Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
44
pubmed:dateCreated
1990-12-31
pubmed:abstractText
Hybrid acute leukaemia is characterized by the presence of lymphoid and myeloid markers in a single cell or in different blast cell subpopulations of the same patient. Authors report on a case of a 14-yr-old girl with hybrid acute leukaemia. Immunofluorescent analysis revealed CD 14, CD 10, CD 19 and HLA-DR antigens in the cell suspension isolated from peripheral blood of the patient. Because of the excess of FAB M1 type blast cells, the patient was treated according to IGCI-1984 protocol. Remission was not achieved despite combined cytotoxic treatment and patient died within 4 weeks following admission. The poor outcome of the disease agrees well with literature data. Hybrid acute leukaemia represents a challenge for the clinical science.
pubmed:language
hun
pubmed:journal
pubmed:citationSubset
IM
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
0030-6002
pubmed:author
pubmed:issnType
Print
pubmed:day
4
pubmed:volume
131
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2431-3
pubmed:dateRevised
2009-10-21
pubmed:meshHeading
pubmed:year
1990
pubmed:articleTitle
[A case of hybrid acute leukemia in a a child].
pubmed:affiliation
Gyermekgyógyászati Klinika, Debreceni Orvostudományi Egyetem.
pubmed:publicationType
Journal Article, English Abstract, Case Reports