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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
|
pubmed:dateCreated |
1992-4-8
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pubmed:abstractText |
Evidence to support the existence of eosinophilic leukemia (EL) as an autonomous eosinophilic proliferation analogous to other myeloproliferative disorders has been somewhat confusing. Partially obscuring the existence of EL as a distinct entity is the proposal that EL merely represents a clinically aggressive form of hypereosinophilic syndrome. This report details the clinical and pathologic findings in a case of EL. The presence of trisomy 8 and trisomy 21; morphologic, cytochemical, and ultrastructural findings of granular abnormalities and nuclear/cytoplasmic dysynchrony; and a clinical course similar to that of other myeloproliferative disorders support the existence of EL as a rare but distinct entity within the spectrum of myeloproliferative diseases.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
|
pubmed:issn |
0886-0238
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
5
|
pubmed:geneSymbol |
bcr-abl
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
195-205
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:1794968-Adult,
pubmed-meshheading:1794968-Biopsy,
pubmed-meshheading:1794968-Bone Marrow,
pubmed-meshheading:1794968-Eosinophilia,
pubmed-meshheading:1794968-Genes, abl,
pubmed-meshheading:1794968-Humans,
pubmed-meshheading:1794968-Karyotyping,
pubmed-meshheading:1794968-Leukemia, Eosinophilic, Acute,
pubmed-meshheading:1794968-Male,
pubmed-meshheading:1794968-Microscopy, Electron,
pubmed-meshheading:1794968-Myeloproliferative Disorders,
pubmed-meshheading:1794968-Syndrome
|
pubmed:year |
1991
|
pubmed:articleTitle |
Eosinophilic leukemia: a myeloproliferative disorder distinct from the hypereosinophilic syndrome.
|
pubmed:affiliation |
Department of Pathology, Medical College of Wisconsin, Milwaukee, WI.
|
pubmed:publicationType |
Journal Article,
Comparative Study,
Case Reports
|