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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
|
pubmed:dateCreated |
1991-3-8
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pubmed:abstractText |
The authors describe a case of idiopathic hypereosinophilic syndrome (HES) terminated as a T-cell lymphoma in a 3-year-old girl. The clinical course was chronic and characterized by chronic eczema, persistent peripheral blood eosinophilia, organomegaly, interstitial lung change, and pericarditis. Postmortem examination demonstrated a disseminated T-cell lymphoma involving the inguinal lymph node, liver, lung, and kidney. The findings of the current case suggest a possibility that certain abnormalities in this case of idiopathic HES per se may have triggered the development of malignant lymphoma, and it may represent a transition of idiopathic HES into a T-cell lymphoma. Other possible sequences are discussed. The development of T-cell malignancy in idiopathic HES in a girl is quite an unusual presentation.
|
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
|
pubmed:issn |
0008-543X
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
15
|
pubmed:volume |
67
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pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
1064-9
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:1991253-Eczema,
pubmed-meshheading:1991253-Eosinophilia,
pubmed-meshheading:1991253-Female,
pubmed-meshheading:1991253-Humans,
pubmed-meshheading:1991253-Infant,
pubmed-meshheading:1991253-Lymphoma, T-Cell,
pubmed-meshheading:1991253-Pericarditis,
pubmed-meshheading:1991253-Syndrome
|
pubmed:year |
1991
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pubmed:articleTitle |
Idiopathic hypereosinophilic syndrome terminating as disseminated T-cell lymphoma.
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pubmed:affiliation |
Department of Pathology, College of Medicine, Seoul National University, Korea.
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pubmed:publicationType |
Journal Article,
Case Reports
|