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Cytomegalovirus reactivation triggers the late onset of hyperthyroidism after autologous peripheral blood transplantation

Thyroid dysfunction is an important issue in patients receiving autologous and allogenic hematopoietic stem cell transplantation (HSCT). However, the exact mechanisms underlying thyrotoxicosis secondary to HSCT remain unclear. The present case exhibited a reversed imbalance in helper/suppressor T-ce...

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Autores principales: Oka, Satoko, Ono, Kazuo, Nohgawa, Masaharu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6260443/
https://www.ncbi.nlm.nih.gov/pubmed/30533381
http://dx.doi.org/10.1016/j.lrr.2018.11.002
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author Oka, Satoko
Ono, Kazuo
Nohgawa, Masaharu
author_facet Oka, Satoko
Ono, Kazuo
Nohgawa, Masaharu
author_sort Oka, Satoko
collection PubMed
description Thyroid dysfunction is an important issue in patients receiving autologous and allogenic hematopoietic stem cell transplantation (HSCT). However, the exact mechanisms underlying thyrotoxicosis secondary to HSCT remain unclear. The present case exhibited a reversed imbalance in helper/suppressor T-cell populations and B-cell dysregulation for a long time after transplantation, and the reactivation of cytomegalovirus may have been associated with the development of clinical hyperthyroidism. The long-term monitoring of thyroid function, T-cell populations, and cytomegalovirus after HSCT is important.
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spelling pubmed-62604432018-12-07 Cytomegalovirus reactivation triggers the late onset of hyperthyroidism after autologous peripheral blood transplantation Oka, Satoko Ono, Kazuo Nohgawa, Masaharu Leuk Res Rep Article Thyroid dysfunction is an important issue in patients receiving autologous and allogenic hematopoietic stem cell transplantation (HSCT). However, the exact mechanisms underlying thyrotoxicosis secondary to HSCT remain unclear. The present case exhibited a reversed imbalance in helper/suppressor T-cell populations and B-cell dysregulation for a long time after transplantation, and the reactivation of cytomegalovirus may have been associated with the development of clinical hyperthyroidism. The long-term monitoring of thyroid function, T-cell populations, and cytomegalovirus after HSCT is important. Elsevier 2018-11-22 /pmc/articles/PMC6260443/ /pubmed/30533381 http://dx.doi.org/10.1016/j.lrr.2018.11.002 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Oka, Satoko
Ono, Kazuo
Nohgawa, Masaharu
Cytomegalovirus reactivation triggers the late onset of hyperthyroidism after autologous peripheral blood transplantation
title Cytomegalovirus reactivation triggers the late onset of hyperthyroidism after autologous peripheral blood transplantation
title_full Cytomegalovirus reactivation triggers the late onset of hyperthyroidism after autologous peripheral blood transplantation
title_fullStr Cytomegalovirus reactivation triggers the late onset of hyperthyroidism after autologous peripheral blood transplantation
title_full_unstemmed Cytomegalovirus reactivation triggers the late onset of hyperthyroidism after autologous peripheral blood transplantation
title_short Cytomegalovirus reactivation triggers the late onset of hyperthyroidism after autologous peripheral blood transplantation
title_sort cytomegalovirus reactivation triggers the late onset of hyperthyroidism after autologous peripheral blood transplantation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6260443/
https://www.ncbi.nlm.nih.gov/pubmed/30533381
http://dx.doi.org/10.1016/j.lrr.2018.11.002
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