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Persistence of Natural Killer (NK) cell lymphocytosis with hyposplenism without development of leukaemia

BACKGROUND: Natural killer (NK) cell lymphocytosis usually has an indolent course and can progress into massive lymphocytosis with development of cytopenias and neoplastic diseases. NK-cells usually express one or more "NK-associated" antigens (CD16, CD56, CD57). Reactive expansions are se...

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Detalles Bibliográficos
Autores principales: Khan, Sujoy, Myers, K
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1215478/
https://www.ncbi.nlm.nih.gov/pubmed/16146576
http://dx.doi.org/10.1186/1472-6890-5-8
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author Khan, Sujoy
Myers, K
author_facet Khan, Sujoy
Myers, K
author_sort Khan, Sujoy
collection PubMed
description BACKGROUND: Natural killer (NK) cell lymphocytosis usually has an indolent course and can progress into massive lymphocytosis with development of cytopenias and neoplastic diseases. NK-cells usually express one or more "NK-associated" antigens (CD16, CD56, CD57). Reactive expansions are seen in autoimmune diseases, viral infections, solid tumours and non-Hodgkin's lymphoma. CASE PRESENTATION: We report a lady with a benign clinical course over 10 years and persistent CD8+/CD3-/CD57+/CD16+ LGL proliferation with presence of Howell-Jolly bodies (functional hyposplenism), an association not previously described. CONCLUSION: We discuss the possible causes of clonal expansion and conclude that this may be part of the spectrum of immune dysregulation associated with NK-cell lymphocytosis.
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spelling pubmed-12154782005-09-17 Persistence of Natural Killer (NK) cell lymphocytosis with hyposplenism without development of leukaemia Khan, Sujoy Myers, K BMC Clin Pathol Case Report BACKGROUND: Natural killer (NK) cell lymphocytosis usually has an indolent course and can progress into massive lymphocytosis with development of cytopenias and neoplastic diseases. NK-cells usually express one or more "NK-associated" antigens (CD16, CD56, CD57). Reactive expansions are seen in autoimmune diseases, viral infections, solid tumours and non-Hodgkin's lymphoma. CASE PRESENTATION: We report a lady with a benign clinical course over 10 years and persistent CD8+/CD3-/CD57+/CD16+ LGL proliferation with presence of Howell-Jolly bodies (functional hyposplenism), an association not previously described. CONCLUSION: We discuss the possible causes of clonal expansion and conclude that this may be part of the spectrum of immune dysregulation associated with NK-cell lymphocytosis. BioMed Central 2005-09-07 /pmc/articles/PMC1215478/ /pubmed/16146576 http://dx.doi.org/10.1186/1472-6890-5-8 Text en Copyright © 2005 Khan and Myers; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Khan, Sujoy
Myers, K
Persistence of Natural Killer (NK) cell lymphocytosis with hyposplenism without development of leukaemia
title Persistence of Natural Killer (NK) cell lymphocytosis with hyposplenism without development of leukaemia
title_full Persistence of Natural Killer (NK) cell lymphocytosis with hyposplenism without development of leukaemia
title_fullStr Persistence of Natural Killer (NK) cell lymphocytosis with hyposplenism without development of leukaemia
title_full_unstemmed Persistence of Natural Killer (NK) cell lymphocytosis with hyposplenism without development of leukaemia
title_short Persistence of Natural Killer (NK) cell lymphocytosis with hyposplenism without development of leukaemia
title_sort persistence of natural killer (nk) cell lymphocytosis with hyposplenism without development of leukaemia
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1215478/
https://www.ncbi.nlm.nih.gov/pubmed/16146576
http://dx.doi.org/10.1186/1472-6890-5-8
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