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- Publisher Website: 10.1093/ajcp/94.2.211
- Scopus: eid_2-s2.0-0025375530
- PMID: 1695480
- WOS: WOS:A1990DR25700015
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Article: A patient with large granular lymphocytosis of unusual phenotype and polymorphic T-cell receptor beta-chain gene rearrangement
Title | A patient with large granular lymphocytosis of unusual phenotype and polymorphic T-cell receptor beta-chain gene rearrangement |
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Authors | |
Keywords | Large granular lymphocytosis Polymorphic T-cell receptor Beta-chain gene rearrangement |
Issue Date | 1990 |
Publisher | American Society for Clinical Pathology. The Journal's web site is located at http://www.ajcp.com |
Citation | American Journal Of Clinical Pathology, 1990, v. 94 n. 2, p. 211-216 How to Cite? |
Abstract | The authors describe a patient with large granular lymphocytosis who presented with fever of unknown origin and jaundice. Immunophenotyping showed that most of the large granular lymphocytes (LGLs) were CD3-, CD16-, and NKH-1 (Leu-19)+ lymphocytes. Lymphocytosis of this subset of LGLs has not been reported. Analysis of T-cell receptor gene showed polymorphic T-cell receptor beta-chain (TCRβ) gene configuration. Functional studies showed reduced natural killer cell function. The clinical course was very aggressive and resistant to chemotherapy. These features again rise the controversial issues of the ontogeny and heterogeneity of LGLs and their relationship to natural killer cells and T-cells. |
Persistent Identifier | http://hdl.handle.net/10722/161847 |
ISSN | 2023 Impact Factor: 2.3 2023 SCImago Journal Rankings: 0.775 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Lin, CK | en_US |
dc.contributor.author | Liu, HW | en_US |
dc.contributor.author | Tse, PWT | en_US |
dc.contributor.author | Lai, CL | en_US |
dc.contributor.author | Chan, GTC | en_US |
dc.date.accessioned | 2012-09-05T05:15:29Z | - |
dc.date.available | 2012-09-05T05:15:29Z | - |
dc.date.issued | 1990 | en_US |
dc.identifier.citation | American Journal Of Clinical Pathology, 1990, v. 94 n. 2, p. 211-216 | en_US |
dc.identifier.issn | 0002-9173 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/161847 | - |
dc.description.abstract | The authors describe a patient with large granular lymphocytosis who presented with fever of unknown origin and jaundice. Immunophenotyping showed that most of the large granular lymphocytes (LGLs) were CD3-, CD16-, and NKH-1 (Leu-19)+ lymphocytes. Lymphocytosis of this subset of LGLs has not been reported. Analysis of T-cell receptor gene showed polymorphic T-cell receptor beta-chain (TCRβ) gene configuration. Functional studies showed reduced natural killer cell function. The clinical course was very aggressive and resistant to chemotherapy. These features again rise the controversial issues of the ontogeny and heterogeneity of LGLs and their relationship to natural killer cells and T-cells. | en_US |
dc.language | eng | en_US |
dc.publisher | American Society for Clinical Pathology. The Journal's web site is located at http://www.ajcp.com | en_US |
dc.relation.ispartof | American Journal of Clinical Pathology | en_US |
dc.subject | Large granular lymphocytosis | - |
dc.subject | Polymorphic T-cell receptor Beta-chain gene rearrangement | - |
dc.subject.mesh | Adult | en_US |
dc.subject.mesh | Antibodies, Monoclonal - Diagnostic Use | en_US |
dc.subject.mesh | Fluorescent Antibody Technique | en_US |
dc.subject.mesh | Gene Rearrangement, Beta-Chain T-Cell Antigen Receptor | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Killer Cells, Natural - Physiology | en_US |
dc.subject.mesh | Lymphocytosis - Genetics - Immunology - Pathology | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Microscopy, Electron | en_US |
dc.subject.mesh | Phenotype | en_US |
dc.subject.mesh | Staining And Labeling | en_US |
dc.subject.mesh | T-Lymphocytes - Pathology - Ultrastructure | en_US |
dc.title | A patient with large granular lymphocytosis of unusual phenotype and polymorphic T-cell receptor beta-chain gene rearrangement | en_US |
dc.type | Article | en_US |
dc.identifier.email | Lai, CL:hrmelcl@hku.hk | en_US |
dc.identifier.authority | Lai, CL=rp00314 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1093/ajcp/94.2.211 | - |
dc.identifier.pmid | 1695480 | - |
dc.identifier.scopus | eid_2-s2.0-0025375530 | en_US |
dc.identifier.volume | 94 | en_US |
dc.identifier.issue | 2 | en_US |
dc.identifier.spage | 211 | en_US |
dc.identifier.epage | 216 | en_US |
dc.identifier.isi | WOS:A1990DR25700015 | - |
dc.publisher.place | United States | en_US |
dc.identifier.scopusauthorid | Lin, CK=15034856400 | en_US |
dc.identifier.scopusauthorid | Liu, HW=36071958800 | en_US |
dc.identifier.scopusauthorid | Tse, PWT=36952697600 | en_US |
dc.identifier.scopusauthorid | Lai, CL=7403086396 | en_US |
dc.identifier.scopusauthorid | Chan, GTC=7202355262 | en_US |
dc.identifier.issnl | 0002-9173 | - |