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A Case Series of Refractory Cutaneous Sarcoidosis Successfully Treated with Infliximab

INTRODUCTION: Sarcoidosis is a systemic granulomatous disease of unknown cause. The management of sarcoidosis remains problematic. Systemic and topical corticosteroids are the mainstay of therapy but may cause unacceptable side effects. Biologic therapies, such as infliximab, have recently been prop...

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Detalles Bibliográficos
Autores principales: Tuchinda, Papapit, Bremmer, Matthew, Gaspari, Anthony A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Healthcare Communications 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3510393/
https://www.ncbi.nlm.nih.gov/pubmed/23205333
http://dx.doi.org/10.1007/s13555-012-0011-9
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author Tuchinda, Papapit
Bremmer, Matthew
Gaspari, Anthony A.
author_facet Tuchinda, Papapit
Bremmer, Matthew
Gaspari, Anthony A.
author_sort Tuchinda, Papapit
collection PubMed
description INTRODUCTION: Sarcoidosis is a systemic granulomatous disease of unknown cause. The management of sarcoidosis remains problematic. Systemic and topical corticosteroids are the mainstay of therapy but may cause unacceptable side effects. Biologic therapies, such as infliximab, have recently been proposed as another treatment option for cutaneous sarcoidosis. CASE REPORT: The authors describe three patients who were diagnosed with cutaneous sarcoidosis with systemic involvement. All of the patients were refractory to conventional therapies but responded to infliximab therapy. CONCLUSION: Infliximab is an alternative medication for refractory sarcoidosis that has a relatively benign side-effect profile. However, definite indications, dosage, interval, and duration of treatment for cutaneous sarcoidosis are not firmly established.
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spelling pubmed-35103932012-11-30 A Case Series of Refractory Cutaneous Sarcoidosis Successfully Treated with Infliximab Tuchinda, Papapit Bremmer, Matthew Gaspari, Anthony A. Dermatol Ther (Heidelb) Case Report INTRODUCTION: Sarcoidosis is a systemic granulomatous disease of unknown cause. The management of sarcoidosis remains problematic. Systemic and topical corticosteroids are the mainstay of therapy but may cause unacceptable side effects. Biologic therapies, such as infliximab, have recently been proposed as another treatment option for cutaneous sarcoidosis. CASE REPORT: The authors describe three patients who were diagnosed with cutaneous sarcoidosis with systemic involvement. All of the patients were refractory to conventional therapies but responded to infliximab therapy. CONCLUSION: Infliximab is an alternative medication for refractory sarcoidosis that has a relatively benign side-effect profile. However, definite indications, dosage, interval, and duration of treatment for cutaneous sarcoidosis are not firmly established. Springer Healthcare Communications 2012-07-26 /pmc/articles/PMC3510393/ /pubmed/23205333 http://dx.doi.org/10.1007/s13555-012-0011-9 Text en © The Author(s) 2012 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Case Report
Tuchinda, Papapit
Bremmer, Matthew
Gaspari, Anthony A.
A Case Series of Refractory Cutaneous Sarcoidosis Successfully Treated with Infliximab
title A Case Series of Refractory Cutaneous Sarcoidosis Successfully Treated with Infliximab
title_full A Case Series of Refractory Cutaneous Sarcoidosis Successfully Treated with Infliximab
title_fullStr A Case Series of Refractory Cutaneous Sarcoidosis Successfully Treated with Infliximab
title_full_unstemmed A Case Series of Refractory Cutaneous Sarcoidosis Successfully Treated with Infliximab
title_short A Case Series of Refractory Cutaneous Sarcoidosis Successfully Treated with Infliximab
title_sort case series of refractory cutaneous sarcoidosis successfully treated with infliximab
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3510393/
https://www.ncbi.nlm.nih.gov/pubmed/23205333
http://dx.doi.org/10.1007/s13555-012-0011-9
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