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Allopurinol-Induced Toxic Epidermal Necrolysis
Toxic epidermal necrolysis (TEN) is an extremely rare condition characterized by separation of dermoepidermal junctions, necrosis, and subsequent detachment of the epidermis over large cutaneous areas. TEN can emerge after exposure to certain medications such as allopurinol, aromatic anticonvulsants...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6757070/ https://www.ncbi.nlm.nih.gov/pubmed/31549231 http://dx.doi.org/10.1007/s40800-019-0101-z |
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author | Buenrostro-Rubio, Ignacio Silva-Villaseñor, José Antonio Hatami-Blechner, Avi William Salazar-del Valle, Juan J Vázquez-Cárdenas, Norma Alejandra Bustamante-Montes, Lilia Patricia González-Alvarez, Rafael |
author_facet | Buenrostro-Rubio, Ignacio Silva-Villaseñor, José Antonio Hatami-Blechner, Avi William Salazar-del Valle, Juan J Vázquez-Cárdenas, Norma Alejandra Bustamante-Montes, Lilia Patricia González-Alvarez, Rafael |
author_sort | Buenrostro-Rubio, Ignacio |
collection | PubMed |
description | Toxic epidermal necrolysis (TEN) is an extremely rare condition characterized by separation of dermoepidermal junctions, necrosis, and subsequent detachment of the epidermis over large cutaneous areas. TEN can emerge after exposure to certain medications such as allopurinol, aromatic anticonvulsants, NSAIDs, nevirapine, and antibacterial sulfonamides. There is no standard protocol for TEN, and the therapy of choice varies from one patient to another. Some of these therapies include silver-releasing wraps/dressings, glucocorticoids, antibodies to inhibit Fas-mediated keratinocyte apoptosis, and cyclosporine A. A 35-year-old male with an allergy to antibacterial sulfonamides who was being treated for arterial hypertension and hyperuricemia with captopril and allopurinol, respectively, was admitted to hospital. The patient showed skin detachment affecting approximately 95% of his surface area, including his face, upper and lower extremities, trunk, back, oropharyngeal mucosa, anal mucosa, ocular mucosa, and genital mucosa. Intravenous methylprednisolone at a dosage of 40 mg/day for 7 days along with abrasive cures was found to be an appropriate treatment in this case. |
format | Online Article Text |
id | pubmed-6757070 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-67570702019-10-07 Allopurinol-Induced Toxic Epidermal Necrolysis Buenrostro-Rubio, Ignacio Silva-Villaseñor, José Antonio Hatami-Blechner, Avi William Salazar-del Valle, Juan J Vázquez-Cárdenas, Norma Alejandra Bustamante-Montes, Lilia Patricia González-Alvarez, Rafael Drug Saf Case Rep Case Report Toxic epidermal necrolysis (TEN) is an extremely rare condition characterized by separation of dermoepidermal junctions, necrosis, and subsequent detachment of the epidermis over large cutaneous areas. TEN can emerge after exposure to certain medications such as allopurinol, aromatic anticonvulsants, NSAIDs, nevirapine, and antibacterial sulfonamides. There is no standard protocol for TEN, and the therapy of choice varies from one patient to another. Some of these therapies include silver-releasing wraps/dressings, glucocorticoids, antibodies to inhibit Fas-mediated keratinocyte apoptosis, and cyclosporine A. A 35-year-old male with an allergy to antibacterial sulfonamides who was being treated for arterial hypertension and hyperuricemia with captopril and allopurinol, respectively, was admitted to hospital. The patient showed skin detachment affecting approximately 95% of his surface area, including his face, upper and lower extremities, trunk, back, oropharyngeal mucosa, anal mucosa, ocular mucosa, and genital mucosa. Intravenous methylprednisolone at a dosage of 40 mg/day for 7 days along with abrasive cures was found to be an appropriate treatment in this case. Springer International Publishing 2019-09-23 /pmc/articles/PMC6757070/ /pubmed/31549231 http://dx.doi.org/10.1007/s40800-019-0101-z Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/), which permits any noncommercial use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Case Report Buenrostro-Rubio, Ignacio Silva-Villaseñor, José Antonio Hatami-Blechner, Avi William Salazar-del Valle, Juan J Vázquez-Cárdenas, Norma Alejandra Bustamante-Montes, Lilia Patricia González-Alvarez, Rafael Allopurinol-Induced Toxic Epidermal Necrolysis |
title | Allopurinol-Induced Toxic Epidermal Necrolysis |
title_full | Allopurinol-Induced Toxic Epidermal Necrolysis |
title_fullStr | Allopurinol-Induced Toxic Epidermal Necrolysis |
title_full_unstemmed | Allopurinol-Induced Toxic Epidermal Necrolysis |
title_short | Allopurinol-Induced Toxic Epidermal Necrolysis |
title_sort | allopurinol-induced toxic epidermal necrolysis |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6757070/ https://www.ncbi.nlm.nih.gov/pubmed/31549231 http://dx.doi.org/10.1007/s40800-019-0101-z |
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