Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
10
|
pubmed:dateCreated |
1993-11-15
|
pubmed:abstractText |
We describe a fatal case of infectious mononucleosis presenting with fulminant hepatic failure associated with extensive CD8-positive lymphocyte infiltration and diffuse karyorrhexis in the liver. Immunohistochemical analysis of mononuclear cells showed that Leu-2a (CD8)-positive lymphocytes were heavily distributed in the portal areas and the sinusoidal spaces, but Leu-3a (CD4)-, Leu-14 (CD22)-, or My 4 (CD14)-positive cells were undetectable in sections of the liver. Southern blot hybridization studies disclosed the presence of Epstein-Barr virus DNA fragments in the liver tissue. The unusual pathologic and immunologic responses observed in this case could not simply be explained by severe Epstein-Barr virus infection. Some superimposed factors should be considered.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Oct
|
pubmed:issn |
0046-8177
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
24
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
1135-9
|
pubmed:dateRevised |
2004-11-17
|
pubmed:meshHeading |
pubmed-meshheading:8406423-Antigens, CD8,
pubmed-meshheading:8406423-Fatal Outcome,
pubmed-meshheading:8406423-Hepatic Encephalopathy,
pubmed-meshheading:8406423-Humans,
pubmed-meshheading:8406423-Infant,
pubmed-meshheading:8406423-Infectious Mononucleosis,
pubmed-meshheading:8406423-Liver,
pubmed-meshheading:8406423-Lymph Nodes,
pubmed-meshheading:8406423-Lymphocyte Activation,
pubmed-meshheading:8406423-Male,
pubmed-meshheading:8406423-T-Lymphocyte Subsets
|
pubmed:year |
1993
|
pubmed:articleTitle |
A case of fatal infectious mononucleosis presenting with fulminant hepatic failure associated with an extensive CD8-positive lymphocyte infiltration in the liver.
|
pubmed:affiliation |
Department of Pediatrics, Akita University School of Medicine, Japan.
|
pubmed:publicationType |
Journal Article,
Case Reports
|