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Treatment of pretibial myxedema with intralesional immunomodulating therapy
OBJECTIVE: Local immune regulation therapy has been one of the therapeutic methods used for the treatment of autoimmune thyroid disease in patients with pretibial myxedema (PTM). However, the poor response rate and high recurrence rate are still major problems. Whether a premixed corticosteroid, com...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5598751/ https://www.ncbi.nlm.nih.gov/pubmed/28932121 http://dx.doi.org/10.2147/TCRM.S143711 |
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author | Ren, Ziwei He, Min Deng, Fang Chen, Yan Chai, Liyin Chen, Bing Deng, Wuquan |
author_facet | Ren, Ziwei He, Min Deng, Fang Chen, Yan Chai, Liyin Chen, Bing Deng, Wuquan |
author_sort | Ren, Ziwei |
collection | PubMed |
description | OBJECTIVE: Local immune regulation therapy has been one of the therapeutic methods used for the treatment of autoimmune thyroid disease in patients with pretibial myxedema (PTM). However, the poor response rate and high recurrence rate are still major problems. Whether a premixed corticosteroid, compound betamethasone, could enhance remission rate and decrease recurrence rate in patients with PTM was investigated in the present study. SUBJECTS AND METHODS: We have performed a clinical utility observation of compound betamethasone with intralesional injections based on basic thyroid disease treatment in 32 PTM patients between January 2008 and August 2016. The patients were followed up for 2 years, and the clinical outcomes and side effects were calculated and analyzed. RESULTS: All patients had a complete remission after different times of injection. A total of 21.7% patients had complete remission with one time of injection, 34.8% with two times of injection, 17.4% with three times of injection, 4.3% with four times of injection, and 4.3% with five times of injection. In all, 56.3% patients with a disease duration of <6 months had complete remission after a 1-month treatment, 37.5% patients with a disease duration between 6 months and 12 months had complete remission after a 2-month treatment, 3.1% patients with a disease duration of 2 years had complete remission after a 5-month treatment, and 3.1% with a disease duration of 5 years had complete remission after a 7-month treatment. CONCLUSION: Compound betamethasone with multipoint intralesional injection is a feasible, effective, and secure novel strategy in the treatment of PTM. |
format | Online Article Text |
id | pubmed-5598751 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-55987512017-09-20 Treatment of pretibial myxedema with intralesional immunomodulating therapy Ren, Ziwei He, Min Deng, Fang Chen, Yan Chai, Liyin Chen, Bing Deng, Wuquan Ther Clin Risk Manag Original Research OBJECTIVE: Local immune regulation therapy has been one of the therapeutic methods used for the treatment of autoimmune thyroid disease in patients with pretibial myxedema (PTM). However, the poor response rate and high recurrence rate are still major problems. Whether a premixed corticosteroid, compound betamethasone, could enhance remission rate and decrease recurrence rate in patients with PTM was investigated in the present study. SUBJECTS AND METHODS: We have performed a clinical utility observation of compound betamethasone with intralesional injections based on basic thyroid disease treatment in 32 PTM patients between January 2008 and August 2016. The patients were followed up for 2 years, and the clinical outcomes and side effects were calculated and analyzed. RESULTS: All patients had a complete remission after different times of injection. A total of 21.7% patients had complete remission with one time of injection, 34.8% with two times of injection, 17.4% with three times of injection, 4.3% with four times of injection, and 4.3% with five times of injection. In all, 56.3% patients with a disease duration of <6 months had complete remission after a 1-month treatment, 37.5% patients with a disease duration between 6 months and 12 months had complete remission after a 2-month treatment, 3.1% patients with a disease duration of 2 years had complete remission after a 5-month treatment, and 3.1% with a disease duration of 5 years had complete remission after a 7-month treatment. CONCLUSION: Compound betamethasone with multipoint intralesional injection is a feasible, effective, and secure novel strategy in the treatment of PTM. Dove Medical Press 2017-09-08 /pmc/articles/PMC5598751/ /pubmed/28932121 http://dx.doi.org/10.2147/TCRM.S143711 Text en © 2017 Ren et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Ren, Ziwei He, Min Deng, Fang Chen, Yan Chai, Liyin Chen, Bing Deng, Wuquan Treatment of pretibial myxedema with intralesional immunomodulating therapy |
title | Treatment of pretibial myxedema with intralesional immunomodulating therapy |
title_full | Treatment of pretibial myxedema with intralesional immunomodulating therapy |
title_fullStr | Treatment of pretibial myxedema with intralesional immunomodulating therapy |
title_full_unstemmed | Treatment of pretibial myxedema with intralesional immunomodulating therapy |
title_short | Treatment of pretibial myxedema with intralesional immunomodulating therapy |
title_sort | treatment of pretibial myxedema with intralesional immunomodulating therapy |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5598751/ https://www.ncbi.nlm.nih.gov/pubmed/28932121 http://dx.doi.org/10.2147/TCRM.S143711 |
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