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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
|
pubmed:dateCreated |
1992-6-19
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pubmed:abstractText |
We report the findings in 21 Belgian patients (12 males and 9 females, median age 61 years) with LGLPD. Symptoms at presentation included infection (n = 9), weight loss (n = 5), asthenia (n = 9), pruritus (n = 2) and arthralgia (n = 7). Four patients were asymptomatic. The main clinical findings were hepatomegaly (n = 5), splenomegaly (n = 8), lymph node enlargement (n = 3) and arthritis (n = 5). All patients had an increased LGL count associated with anemia (n = 12), neutropenia (n = 17), often less than 0.5.10(9)/L (n = 10) and thrombocytopenia (n = 6). Three patterns of lymphocyte surface markers were observed: CD3+CD4-8+ (14 patients), CD3+CD4-8+ (5 patients) and CD3+CD4+8- (1 patient). An abnormal karyotype was found in 2 patients. T-cell receptor gene was rearranged in all cases tested (9/9).
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
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pubmed:issn |
0001-5512
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
47
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pubmed:owner |
NLM
|
pubmed:authorsComplete |
N
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pubmed:pagination |
21-9
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pubmed:dateRevised |
2005-11-16
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pubmed:meshHeading |
pubmed-meshheading:1317080-Adult,
pubmed-meshheading:1317080-Aged,
pubmed-meshheading:1317080-Female,
pubmed-meshheading:1317080-Humans,
pubmed-meshheading:1317080-Karyotyping,
pubmed-meshheading:1317080-Lymphoproliferative Disorders,
pubmed-meshheading:1317080-Male,
pubmed-meshheading:1317080-Middle Aged,
pubmed-meshheading:1317080-Phenotype,
pubmed-meshheading:1317080-T-Lymphocytes
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pubmed:year |
1992
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pubmed:articleTitle |
Large granular lymphocyte proliferative disease: 21 Belgian cases and review of the literature.
|
pubmed:affiliation |
Hôpital de Jolimont, La Louvière, Bruxelles.
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pubmed:publicationType |
Journal Article,
Review
|