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A Randomized Controlled Trial of Intralesional Glucocorticoid for Treating Pretibial Myxedema
BACKGROUND: Pretibial myxedema (PTM) is an uncommon dermopathy associated with autoimmune thyroid diseases. Now it is thought to be autoimmune and its treatment with glucocorticoid is helpful. However, it has not been evaluated. METHODS: A prospective randomized controlled trial was performed in 110...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elmer Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4596268/ https://www.ncbi.nlm.nih.gov/pubmed/26491499 http://dx.doi.org/10.14740/jocmr2303w |
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author | Lan, Changgui Li, Can Chen, Wei Mei, Xiaofeng Zhao, Jing Hu, Jie |
author_facet | Lan, Changgui Li, Can Chen, Wei Mei, Xiaofeng Zhao, Jing Hu, Jie |
author_sort | Lan, Changgui |
collection | PubMed |
description | BACKGROUND: Pretibial myxedema (PTM) is an uncommon dermopathy associated with autoimmune thyroid diseases. Now it is thought to be autoimmune and its treatment with glucocorticoid is helpful. However, it has not been evaluated. METHODS: A prospective randomized controlled trial was performed in 110 patients with PTM to evaluate the efficacy and safety of triamcinolone acetonide with intralesional injection once every 3 days and once every 7 days. Randomization was performed with drawing lots and it was also stratified according to variants of PTM lesions. In the follow-up, recurrent rates were observed. The SPSS Statistics 17.0 Software was used in the statistical analysis. RESULTS: The complete response rates were 78.2%, 83.6%, and 87.3% in regimen 1 and 50.9%, 89.1%, and 90.9% in regimen 2 at 3 weeks, 7 weeks and the end of therapy, respectively. Regimen 1 had an earlier efficacy than regimen 2, but at 7 weeks and end of therapy, there were no differences between two regimens. The majority of non-severe variants got complete response but severe variants did not. The adverse reaction rates in regimen 1 were higher and earlier than those in regimen 2. Adverse reaction occurring time in regimen 1 was shorter than that in regimen 2. Recurrent rates were 31.25% and 32% in regimens 1 and 2 at 3.5-year follow-up. CONCLUSIONS: For its autoimmune, hyperplasia and disabled features, early treatment of PTM with glucocorticoid is necessary to get complete response. Dosage and frequency of intralesional steroid injection and lesional variants influence the efficacy of PTM. Once every 7 days is a better regimen. |
format | Online Article Text |
id | pubmed-4596268 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Elmer Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-45962682015-10-21 A Randomized Controlled Trial of Intralesional Glucocorticoid for Treating Pretibial Myxedema Lan, Changgui Li, Can Chen, Wei Mei, Xiaofeng Zhao, Jing Hu, Jie J Clin Med Res Original Article BACKGROUND: Pretibial myxedema (PTM) is an uncommon dermopathy associated with autoimmune thyroid diseases. Now it is thought to be autoimmune and its treatment with glucocorticoid is helpful. However, it has not been evaluated. METHODS: A prospective randomized controlled trial was performed in 110 patients with PTM to evaluate the efficacy and safety of triamcinolone acetonide with intralesional injection once every 3 days and once every 7 days. Randomization was performed with drawing lots and it was also stratified according to variants of PTM lesions. In the follow-up, recurrent rates were observed. The SPSS Statistics 17.0 Software was used in the statistical analysis. RESULTS: The complete response rates were 78.2%, 83.6%, and 87.3% in regimen 1 and 50.9%, 89.1%, and 90.9% in regimen 2 at 3 weeks, 7 weeks and the end of therapy, respectively. Regimen 1 had an earlier efficacy than regimen 2, but at 7 weeks and end of therapy, there were no differences between two regimens. The majority of non-severe variants got complete response but severe variants did not. The adverse reaction rates in regimen 1 were higher and earlier than those in regimen 2. Adverse reaction occurring time in regimen 1 was shorter than that in regimen 2. Recurrent rates were 31.25% and 32% in regimens 1 and 2 at 3.5-year follow-up. CONCLUSIONS: For its autoimmune, hyperplasia and disabled features, early treatment of PTM with glucocorticoid is necessary to get complete response. Dosage and frequency of intralesional steroid injection and lesional variants influence the efficacy of PTM. Once every 7 days is a better regimen. Elmer Press 2015-11 2015-09-25 /pmc/articles/PMC4596268/ /pubmed/26491499 http://dx.doi.org/10.14740/jocmr2303w Text en Copyright 2015, Lan et al. http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Lan, Changgui Li, Can Chen, Wei Mei, Xiaofeng Zhao, Jing Hu, Jie A Randomized Controlled Trial of Intralesional Glucocorticoid for Treating Pretibial Myxedema |
title | A Randomized Controlled Trial of Intralesional Glucocorticoid for Treating Pretibial Myxedema |
title_full | A Randomized Controlled Trial of Intralesional Glucocorticoid for Treating Pretibial Myxedema |
title_fullStr | A Randomized Controlled Trial of Intralesional Glucocorticoid for Treating Pretibial Myxedema |
title_full_unstemmed | A Randomized Controlled Trial of Intralesional Glucocorticoid for Treating Pretibial Myxedema |
title_short | A Randomized Controlled Trial of Intralesional Glucocorticoid for Treating Pretibial Myxedema |
title_sort | randomized controlled trial of intralesional glucocorticoid for treating pretibial myxedema |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4596268/ https://www.ncbi.nlm.nih.gov/pubmed/26491499 http://dx.doi.org/10.14740/jocmr2303w |
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