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A case report of hydralazine-induced skin reaction: Probable toxic epidermal necrolysis (TEN)

Patient: Female, 75 Final Diagnosis: Hypertensive crisis with multi organ failure Symptoms: Anemia • general weakness • hypokalemia • nausea • tachycardia Medication: — Clinical Procedure: — Specialty: Cardiology OBJECTIVE: Unexpected drug reaction BACKGROUND: Skin reactions are common adverse drug...

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Autores principales: Mahfouz, Ahmed, Mahmoud, Ahmed Naguib, Ashfaq, Patel Ahmad, Siyabi, Khalid Hamed Al
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3979803/
https://www.ncbi.nlm.nih.gov/pubmed/24719674
http://dx.doi.org/10.12659/AJCR.890038
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author Mahfouz, Ahmed
Mahmoud, Ahmed Naguib
Ashfaq, Patel Ahmad
Siyabi, Khalid Hamed Al
author_facet Mahfouz, Ahmed
Mahmoud, Ahmed Naguib
Ashfaq, Patel Ahmad
Siyabi, Khalid Hamed Al
author_sort Mahfouz, Ahmed
collection PubMed
description Patient: Female, 75 Final Diagnosis: Hypertensive crisis with multi organ failure Symptoms: Anemia • general weakness • hypokalemia • nausea • tachycardia Medication: — Clinical Procedure: — Specialty: Cardiology OBJECTIVE: Unexpected drug reaction BACKGROUND: Skin reactions are common adverse drug reactions and may include angioedema, erythroderma, Stevens-Johnson syndrome, and toxic epidermal necrolysis (TEN). TEN is a rare but serious reaction characterized by widespread erythema, necrosis, and bullous detachment of the epidermis and mucous membranes. CASE REPORT: An elderly woman presented with generalized weakness and nausea, associated with a hypertensive crisis. Following the initiation of hydralazine, well-demarcated erythematous maculopapular rashes appeared on her right forearm and left leg, which transformed into a bullous rash. Subsequently, a similar patch appeared on her left forearm, with a similar progression and associated with generalized edema of the extremities. A clinical diagnosis of drug-induced toxic epidermal necrolysis was made and hydralazine was discontinued. Following this, the skin lesions improved, with complete subsequent resolution. Skin biopsy was not performed due to the rapid resolution of the lesions. A negative screen for autoantibodies ruled out systemic lupus erythematosus, scleroderma, and other undifferentiated connective tissue disorders. After re-administration of hydralazine, the same lesions appeared again, which again resolved after its discontinuation, thus confirming our initial clinical suspicion. Treatment is immediate discontinuation of the offending drug and supportive care. CONCLUSIONS: Clinical awareness with close monitoring is important for the identification of a rare adverse drug reaction, which can be fatal if not diagnosed and treated promptly.
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spelling pubmed-39798032014-04-09 A case report of hydralazine-induced skin reaction: Probable toxic epidermal necrolysis (TEN) Mahfouz, Ahmed Mahmoud, Ahmed Naguib Ashfaq, Patel Ahmad Siyabi, Khalid Hamed Al Am J Case Rep Articles Patient: Female, 75 Final Diagnosis: Hypertensive crisis with multi organ failure Symptoms: Anemia • general weakness • hypokalemia • nausea • tachycardia Medication: — Clinical Procedure: — Specialty: Cardiology OBJECTIVE: Unexpected drug reaction BACKGROUND: Skin reactions are common adverse drug reactions and may include angioedema, erythroderma, Stevens-Johnson syndrome, and toxic epidermal necrolysis (TEN). TEN is a rare but serious reaction characterized by widespread erythema, necrosis, and bullous detachment of the epidermis and mucous membranes. CASE REPORT: An elderly woman presented with generalized weakness and nausea, associated with a hypertensive crisis. Following the initiation of hydralazine, well-demarcated erythematous maculopapular rashes appeared on her right forearm and left leg, which transformed into a bullous rash. Subsequently, a similar patch appeared on her left forearm, with a similar progression and associated with generalized edema of the extremities. A clinical diagnosis of drug-induced toxic epidermal necrolysis was made and hydralazine was discontinued. Following this, the skin lesions improved, with complete subsequent resolution. Skin biopsy was not performed due to the rapid resolution of the lesions. A negative screen for autoantibodies ruled out systemic lupus erythematosus, scleroderma, and other undifferentiated connective tissue disorders. After re-administration of hydralazine, the same lesions appeared again, which again resolved after its discontinuation, thus confirming our initial clinical suspicion. Treatment is immediate discontinuation of the offending drug and supportive care. CONCLUSIONS: Clinical awareness with close monitoring is important for the identification of a rare adverse drug reaction, which can be fatal if not diagnosed and treated promptly. International Scientific Literature, Inc. 2014-03-31 /pmc/articles/PMC3979803/ /pubmed/24719674 http://dx.doi.org/10.12659/AJCR.890038 Text en © Am J Case Rep, 2014 This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License
spellingShingle Articles
Mahfouz, Ahmed
Mahmoud, Ahmed Naguib
Ashfaq, Patel Ahmad
Siyabi, Khalid Hamed Al
A case report of hydralazine-induced skin reaction: Probable toxic epidermal necrolysis (TEN)
title A case report of hydralazine-induced skin reaction: Probable toxic epidermal necrolysis (TEN)
title_full A case report of hydralazine-induced skin reaction: Probable toxic epidermal necrolysis (TEN)
title_fullStr A case report of hydralazine-induced skin reaction: Probable toxic epidermal necrolysis (TEN)
title_full_unstemmed A case report of hydralazine-induced skin reaction: Probable toxic epidermal necrolysis (TEN)
title_short A case report of hydralazine-induced skin reaction: Probable toxic epidermal necrolysis (TEN)
title_sort case report of hydralazine-induced skin reaction: probable toxic epidermal necrolysis (ten)
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3979803/
https://www.ncbi.nlm.nih.gov/pubmed/24719674
http://dx.doi.org/10.12659/AJCR.890038
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