Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
|
pubmed:dateCreated |
1989-2-1
|
pubmed:abstractText |
A 55-year-old woman had bilateral hilar lymphadenopathy and retinouveitis. Microscopic examination of a biopsy specimen from a mediastinal lymph node revealed noncaseating epithelioid cell granulomas. Since granulomatous diseases of infectious origin and sarcoid reaction were reasonably excluded, she was diagnosed as having pulmonary sarcoidosis. Bronchoalveolar lavage findings were atypical in that the ratio of helper T cells to suppressor T cells (CD4/8 ratio) was 0.5 in two separate examinations, despite a moderately increased proportion of lymphocytes. Immunohistochemical examination of the lymph node also showed a predominancy of suppressor T cells. The inversion of the CD4/8 ratio suggests the presence of heterogeneity in the immunoregulatory mechanism in pulmonary sarcoidosis and may have a prognostic significance.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
AIM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Jan
|
pubmed:issn |
0012-3692
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
95
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
228-31
|
pubmed:dateRevised |
2004-11-17
|
pubmed:meshHeading |
pubmed-meshheading:2491800-Antigens, CD8,
pubmed-meshheading:2491800-Antigens, Differentiation, T-Lymphocyte,
pubmed-meshheading:2491800-Bronchoalveolar Lavage Fluid,
pubmed-meshheading:2491800-Female,
pubmed-meshheading:2491800-Granuloma,
pubmed-meshheading:2491800-Humans,
pubmed-meshheading:2491800-Inflammation,
pubmed-meshheading:2491800-Lung Diseases,
pubmed-meshheading:2491800-Lymph Nodes,
pubmed-meshheading:2491800-Middle Aged,
pubmed-meshheading:2491800-Pulmonary Alveoli,
pubmed-meshheading:2491800-Sarcoidosis,
pubmed-meshheading:2491800-T-Lymphocytes
|
pubmed:year |
1989
|
pubmed:articleTitle |
CD8+ cell-dominant alveolitis in pulmonary sarcoidosis.
|
pubmed:affiliation |
First Department of Medicine, School of Medicine, Hokkaido University Hospital, Sapporo, Japan.
|
pubmed:publicationType |
Journal Article,
Case Reports
|