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Fulvestrant-induced toxic epidermal necrolysis

Toxic epidermal necrolysis is a condition with massive keratinocyte apoptosis, and it is associated with high mortality rates. Fulvestrant, an estrogen receptor antagonist, is indicated in the treatment of estrogen receptor-positive metastatic breast cancer in postmenopausal women. To our knowledge,...

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Autores principales: Morales-Conde, Macarena, López-Ibáñez, Natividad, Calvete-Candenas, Julio, Mendonça, Francisco Manuel Ildefonso
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Dermatologia 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6486080/
https://www.ncbi.nlm.nih.gov/pubmed/31090829
http://dx.doi.org/10.1590/abd1806-4841.20197964
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author Morales-Conde, Macarena
López-Ibáñez, Natividad
Calvete-Candenas, Julio
Mendonça, Francisco Manuel Ildefonso
author_facet Morales-Conde, Macarena
López-Ibáñez, Natividad
Calvete-Candenas, Julio
Mendonça, Francisco Manuel Ildefonso
author_sort Morales-Conde, Macarena
collection PubMed
description Toxic epidermal necrolysis is a condition with massive keratinocyte apoptosis, and it is associated with high mortality rates. Fulvestrant, an estrogen receptor antagonist, is indicated in the treatment of estrogen receptor-positive metastatic breast cancer in postmenopausal women. To our knowledge, this is the first described case of toxic epidermal necrolysis due to fulvestrant. A 56-year-old woman received 500 mg of intramuscular fulvestrant monthly for metastatic ductal carcinoma of the breast. Five days after the first dose, the patient presented with a maculopapular rash that evolved to blisters, and a detachment of the epidermis in over 30% of the total body surface area. Histological analysis was compatible with toxic epidermal necrolysis. Fulvestrant was discontinued, topical management and supportive care were initiated.
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spelling pubmed-64860802019-04-30 Fulvestrant-induced toxic epidermal necrolysis Morales-Conde, Macarena López-Ibáñez, Natividad Calvete-Candenas, Julio Mendonça, Francisco Manuel Ildefonso An Bras Dermatol Case Report Toxic epidermal necrolysis is a condition with massive keratinocyte apoptosis, and it is associated with high mortality rates. Fulvestrant, an estrogen receptor antagonist, is indicated in the treatment of estrogen receptor-positive metastatic breast cancer in postmenopausal women. To our knowledge, this is the first described case of toxic epidermal necrolysis due to fulvestrant. A 56-year-old woman received 500 mg of intramuscular fulvestrant monthly for metastatic ductal carcinoma of the breast. Five days after the first dose, the patient presented with a maculopapular rash that evolved to blisters, and a detachment of the epidermis in over 30% of the total body surface area. Histological analysis was compatible with toxic epidermal necrolysis. Fulvestrant was discontinued, topical management and supportive care were initiated. Sociedade Brasileira de Dermatologia 2019 /pmc/articles/PMC6486080/ /pubmed/31090829 http://dx.doi.org/10.1590/abd1806-4841.20197964 Text en http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivative License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium provided the original work is properly cited and the work is not changed in any way.
spellingShingle Case Report
Morales-Conde, Macarena
López-Ibáñez, Natividad
Calvete-Candenas, Julio
Mendonça, Francisco Manuel Ildefonso
Fulvestrant-induced toxic epidermal necrolysis
title Fulvestrant-induced toxic epidermal necrolysis
title_full Fulvestrant-induced toxic epidermal necrolysis
title_fullStr Fulvestrant-induced toxic epidermal necrolysis
title_full_unstemmed Fulvestrant-induced toxic epidermal necrolysis
title_short Fulvestrant-induced toxic epidermal necrolysis
title_sort fulvestrant-induced toxic epidermal necrolysis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6486080/
https://www.ncbi.nlm.nih.gov/pubmed/31090829
http://dx.doi.org/10.1590/abd1806-4841.20197964
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