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DRESS syndrome associated with type 2 diabetes in a child

Drug rash with eosinophilia and systemic symptoms (DRESS) syndrome is an uncommon, life-threatening drug reaction. The basic findings are skin rash, multiorgan involvement, and eosinophilia. Most of the aromatic anticonvulsants, such as phenytoin, phenobarbital and carbamazepine can induce DRESS. He...

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Autores principales: Erdem, Semiha Bahceci, Nacaroglu, Hikmet Tekin, Bag, Ozlem, Karkiner, Canan Sule Unsal, Korkmaz, Huseyin Anil, Can, Demet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Polish Society of Experimental and Clinical Immunology 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4737734/
https://www.ncbi.nlm.nih.gov/pubmed/26862317
http://dx.doi.org/10.5114/ceji.2015.54606
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author Erdem, Semiha Bahceci
Nacaroglu, Hikmet Tekin
Bag, Ozlem
Karkiner, Canan Sule Unsal
Korkmaz, Huseyin Anil
Can, Demet
author_facet Erdem, Semiha Bahceci
Nacaroglu, Hikmet Tekin
Bag, Ozlem
Karkiner, Canan Sule Unsal
Korkmaz, Huseyin Anil
Can, Demet
author_sort Erdem, Semiha Bahceci
collection PubMed
description Drug rash with eosinophilia and systemic symptoms (DRESS) syndrome is an uncommon, life-threatening drug reaction. The basic findings are skin rash, multiorgan involvement, and eosinophilia. Most of the aromatic anticonvulsants, such as phenytoin, phenobarbital and carbamazepine can induce DRESS. Herein we report a 14-year-old patient with DRESS syndrome related to carbamazepine use. The patient presented with signs of involvement of the skin, lungs, liver, and microscopic hematuria. Carbamazepine treatment was discontinued; antihistamines and steroids were started. Hyperglycemia, commencing on the first dose of the steroid given, persisted even after the discontinuation of steroids and improvement of other signs. There were no signs of pancreatitis or type 1 diabetes clinically in laboratory tests. Her blood glucose levels were regulated at first with insulin and later with metformin. Within 1 year of follow-up, still regulated with oral antidiabetics, she has been diagnosed with type 2 diabetes. Formerly, long-term sequelae related to “drug rash with eosinophilia and systemic symptoms syndrome” such as hepatic and renal failure, type 1 diabetes mellitus, Grave's disease, autoimmune hemolytic anemia, and lupus have also been reported. However, up to date, no cases with type 2 diabetes have been reported as long-term sequelae. To our knowledge, this is the first case in the literature presenting with type 2 diabetes as long-term sequelae.
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spelling pubmed-47377342016-02-09 DRESS syndrome associated with type 2 diabetes in a child Erdem, Semiha Bahceci Nacaroglu, Hikmet Tekin Bag, Ozlem Karkiner, Canan Sule Unsal Korkmaz, Huseyin Anil Can, Demet Cent Eur J Immunol Case Report Drug rash with eosinophilia and systemic symptoms (DRESS) syndrome is an uncommon, life-threatening drug reaction. The basic findings are skin rash, multiorgan involvement, and eosinophilia. Most of the aromatic anticonvulsants, such as phenytoin, phenobarbital and carbamazepine can induce DRESS. Herein we report a 14-year-old patient with DRESS syndrome related to carbamazepine use. The patient presented with signs of involvement of the skin, lungs, liver, and microscopic hematuria. Carbamazepine treatment was discontinued; antihistamines and steroids were started. Hyperglycemia, commencing on the first dose of the steroid given, persisted even after the discontinuation of steroids and improvement of other signs. There were no signs of pancreatitis or type 1 diabetes clinically in laboratory tests. Her blood glucose levels were regulated at first with insulin and later with metformin. Within 1 year of follow-up, still regulated with oral antidiabetics, she has been diagnosed with type 2 diabetes. Formerly, long-term sequelae related to “drug rash with eosinophilia and systemic symptoms syndrome” such as hepatic and renal failure, type 1 diabetes mellitus, Grave's disease, autoimmune hemolytic anemia, and lupus have also been reported. However, up to date, no cases with type 2 diabetes have been reported as long-term sequelae. To our knowledge, this is the first case in the literature presenting with type 2 diabetes as long-term sequelae. Polish Society of Experimental and Clinical Immunology 2016-01-15 2015 /pmc/articles/PMC4737734/ /pubmed/26862317 http://dx.doi.org/10.5114/ceji.2015.54606 Text en Copyright © Central European Journal of Immunology 2016 http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
spellingShingle Case Report
Erdem, Semiha Bahceci
Nacaroglu, Hikmet Tekin
Bag, Ozlem
Karkiner, Canan Sule Unsal
Korkmaz, Huseyin Anil
Can, Demet
DRESS syndrome associated with type 2 diabetes in a child
title DRESS syndrome associated with type 2 diabetes in a child
title_full DRESS syndrome associated with type 2 diabetes in a child
title_fullStr DRESS syndrome associated with type 2 diabetes in a child
title_full_unstemmed DRESS syndrome associated with type 2 diabetes in a child
title_short DRESS syndrome associated with type 2 diabetes in a child
title_sort dress syndrome associated with type 2 diabetes in a child
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4737734/
https://www.ncbi.nlm.nih.gov/pubmed/26862317
http://dx.doi.org/10.5114/ceji.2015.54606
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