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Eltrombopag in Good's Syndrome
Good's syndrome is a rare acquired immunodeficiency associated with thymoma. Eltrombopag is a thrombopoietin receptor agonist and has been shown to be a valuable supplement to the treatment of several types of refractory cytopenias. In this paper, we describe a male patient suffering from Good&...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4217369/ https://www.ncbi.nlm.nih.gov/pubmed/25389501 http://dx.doi.org/10.1155/2014/172139 |
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author | Kristiansen, Håvard Anton Spetalen, Signe Fløisand, Yngvar Heldal, Dag |
author_facet | Kristiansen, Håvard Anton Spetalen, Signe Fløisand, Yngvar Heldal, Dag |
author_sort | Kristiansen, Håvard Anton |
collection | PubMed |
description | Good's syndrome is a rare acquired immunodeficiency associated with thymoma. Eltrombopag is a thrombopoietin receptor agonist and has been shown to be a valuable supplement to the treatment of several types of refractory cytopenias. In this paper, we describe a male patient suffering from Good's syndrome with immune-mediated T-cell driven pancytopenia and absence of megakaryopoiesis. He was successfully treated with eltrombopag resulting in a multilineage clinical response. |
format | Online Article Text |
id | pubmed-4217369 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-42173692014-11-11 Eltrombopag in Good's Syndrome Kristiansen, Håvard Anton Spetalen, Signe Fløisand, Yngvar Heldal, Dag Case Rep Hematol Case Report Good's syndrome is a rare acquired immunodeficiency associated with thymoma. Eltrombopag is a thrombopoietin receptor agonist and has been shown to be a valuable supplement to the treatment of several types of refractory cytopenias. In this paper, we describe a male patient suffering from Good's syndrome with immune-mediated T-cell driven pancytopenia and absence of megakaryopoiesis. He was successfully treated with eltrombopag resulting in a multilineage clinical response. Hindawi Publishing Corporation 2014 2014-10-19 /pmc/articles/PMC4217369/ /pubmed/25389501 http://dx.doi.org/10.1155/2014/172139 Text en Copyright © 2014 Håvard Anton Kristiansen et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Kristiansen, Håvard Anton Spetalen, Signe Fløisand, Yngvar Heldal, Dag Eltrombopag in Good's Syndrome |
title | Eltrombopag in Good's Syndrome |
title_full | Eltrombopag in Good's Syndrome |
title_fullStr | Eltrombopag in Good's Syndrome |
title_full_unstemmed | Eltrombopag in Good's Syndrome |
title_short | Eltrombopag in Good's Syndrome |
title_sort | eltrombopag in good's syndrome |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4217369/ https://www.ncbi.nlm.nih.gov/pubmed/25389501 http://dx.doi.org/10.1155/2014/172139 |
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