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CHILDHOOD VITILIGO: RESPONSE TO METHYLPREDNISOLONE ORAL MINIPULSE THERAPY AND TOPICAL FLUTICASONE COMBINATION
BACKGROUND: Childhood vitiligo is always a challenge to treat, especially when the disease is progressing rapidly in such a patient. Oral minipulse with betamethasone has been tried in childhood vitiligo and also in some other immune mediated skin disorders with good results. AIMS: The aim of the pr...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Medknow Publications
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2807150/ https://www.ncbi.nlm.nih.gov/pubmed/20101306 http://dx.doi.org/10.4103/0019-5154.53185 |
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author | Majid, Imran Masood, Qazi Hassan, Iffat Khan, Dilshad Chisti, Muzammil |
author_facet | Majid, Imran Masood, Qazi Hassan, Iffat Khan, Dilshad Chisti, Muzammil |
author_sort | Majid, Imran |
collection | PubMed |
description | BACKGROUND: Childhood vitiligo is always a challenge to treat, especially when the disease is progressing rapidly in such a patient. Oral minipulse with betamethasone has been tried in childhood vitiligo and also in some other immune mediated skin disorders with good results. AIMS: The aim of the present study was to see the overall efficacy of methylprednisolone oral minipulse therapy in combination with topical fluticasone in progressive childhood vitiligo. The combination was tried to achieve a significant amount of repigmentation of vitiligo lesions already present at the initial visit. MATERIALS AND METHODS: Four hundred children with progressive vitiligo were enrolled for this study and were prescribed oral methylprednisolone on two consecutive days every week in a minipulse form for a period of six months. In addition, the patients were instructed to apply fluticasone ointment topically once a day on their vitiligo lesions. The patients were assessed for the remission achieved as well as the extent of repigmentation of their already existent lesions. RESULTS: More than 90% of patients went into complete remission after the start of the therapy. Moreover, about 65% (two-thirds) of patients achieved good to excellent repigmentation of lesions at the end of six months of therapy. The therapy was also well tolerated and the side effects seen were almost negligible. CONCLUSIONS: Oral minipulse treatment with methylprednisolone is an effective treatment option for controlling the disease spread in childhood vitiligo and with the addition of topical fluticasone the extent of repigmentation achieved is also quite significant. |
format | Text |
id | pubmed-2807150 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Medknow Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-28071502010-01-25 CHILDHOOD VITILIGO: RESPONSE TO METHYLPREDNISOLONE ORAL MINIPULSE THERAPY AND TOPICAL FLUTICASONE COMBINATION Majid, Imran Masood, Qazi Hassan, Iffat Khan, Dilshad Chisti, Muzammil Indian J Dermatol Original Article BACKGROUND: Childhood vitiligo is always a challenge to treat, especially when the disease is progressing rapidly in such a patient. Oral minipulse with betamethasone has been tried in childhood vitiligo and also in some other immune mediated skin disorders with good results. AIMS: The aim of the present study was to see the overall efficacy of methylprednisolone oral minipulse therapy in combination with topical fluticasone in progressive childhood vitiligo. The combination was tried to achieve a significant amount of repigmentation of vitiligo lesions already present at the initial visit. MATERIALS AND METHODS: Four hundred children with progressive vitiligo were enrolled for this study and were prescribed oral methylprednisolone on two consecutive days every week in a minipulse form for a period of six months. In addition, the patients were instructed to apply fluticasone ointment topically once a day on their vitiligo lesions. The patients were assessed for the remission achieved as well as the extent of repigmentation of their already existent lesions. RESULTS: More than 90% of patients went into complete remission after the start of the therapy. Moreover, about 65% (two-thirds) of patients achieved good to excellent repigmentation of lesions at the end of six months of therapy. The therapy was also well tolerated and the side effects seen were almost negligible. CONCLUSIONS: Oral minipulse treatment with methylprednisolone is an effective treatment option for controlling the disease spread in childhood vitiligo and with the addition of topical fluticasone the extent of repigmentation achieved is also quite significant. Medknow Publications 2009 /pmc/articles/PMC2807150/ /pubmed/20101306 http://dx.doi.org/10.4103/0019-5154.53185 Text en © Indian Journal of Dermatology 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 Majid, Imran Masood, Qazi Hassan, Iffat Khan, Dilshad Chisti, Muzammil CHILDHOOD VITILIGO: RESPONSE TO METHYLPREDNISOLONE ORAL MINIPULSE THERAPY AND TOPICAL FLUTICASONE COMBINATION |
title | CHILDHOOD VITILIGO: RESPONSE TO METHYLPREDNISOLONE ORAL MINIPULSE THERAPY AND TOPICAL FLUTICASONE COMBINATION |
title_full | CHILDHOOD VITILIGO: RESPONSE TO METHYLPREDNISOLONE ORAL MINIPULSE THERAPY AND TOPICAL FLUTICASONE COMBINATION |
title_fullStr | CHILDHOOD VITILIGO: RESPONSE TO METHYLPREDNISOLONE ORAL MINIPULSE THERAPY AND TOPICAL FLUTICASONE COMBINATION |
title_full_unstemmed | CHILDHOOD VITILIGO: RESPONSE TO METHYLPREDNISOLONE ORAL MINIPULSE THERAPY AND TOPICAL FLUTICASONE COMBINATION |
title_short | CHILDHOOD VITILIGO: RESPONSE TO METHYLPREDNISOLONE ORAL MINIPULSE THERAPY AND TOPICAL FLUTICASONE COMBINATION |
title_sort | childhood vitiligo: response to methylprednisolone oral minipulse therapy and topical fluticasone combination |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2807150/ https://www.ncbi.nlm.nih.gov/pubmed/20101306 http://dx.doi.org/10.4103/0019-5154.53185 |
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