Successful Combination Therapy Including Plasma Exchange for Severe Toxic Epidermal Necrolysis

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Severe Antiretroviral Therapy-Induced Toxic Epidermal Necrolysis in a Child

Toxic epidermal necrolysis (TEN) is a rare and life-threatening condition characterised by extensive epidermal detachment and mucosal erosion. Adverse drug reaction is a strongly correlated causative factor and TEN is currently considered the most severe end of a spectrum of drug-induced mucocutaneous diseases, including Stevens-Johnson syndrome. Attaining an accurate and detailed patient histo...

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Successful Treatment for Toxic Epidermal Necrolysis/Drug-Induced Hypersensitivity Syndrome Overlap with Corticosteroids, Intravenous Immunoglobulins and Plasma Exchange

An-80-year-old woman treated with allopurinol showed atypical target lesions with blister and erosions, which rapidly extended over the trunk and limb. She was diagnosed as Toxic Epidermal Necrolysis (TEN). Despite the treatment with pulsed corticosteroids and i.v. immunoglobulins, the skin lesions rapidly extended over the entire body. Strikingly, the progression of blistering with stopped by ...

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[Toxic epidermal necrolysis].

Toxic epidermal necrolysis is a potentially fatal dermatological disease. Large bullae covering extensive areas of the body cause continuous exfoliation of skin, which requires immediate medical attention. Intraoral manifestations may precede cutaneous lesions. Two cases with different treatment protocols are presented.

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Toxic Epidermal Necrolysis

Figure 1. Generalized epidermolysis on anterior and posterior torso with crusty erosions on oral mucosa. DESCRIPTION A 33-year-old woman presents with diffuse rash 3 weeks after completing a course of Bactrim for a urinary tract infection. Erythematous maculopapular rash is evident on the trunk and extremities with painful, epidermal sloughing on the back leaving a moist, denuded dermis. Note t...

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Intrapartum Toxic Epidermal Necrolysis.

This syndrome was first described by Lyell (1956) in this country and by Lang and Walker (1956) in South Africa and has since been reported with increasing frequency. Beare (1962), in a comprehensive review, collected 35 cases from the published reports and described 10 further cases that he had observed personally. He suggests that it is unlikely that the syndrome could have been seen in the U...

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ژورنال

عنوان ژورنال: Journal of General and Family Medicine

سال: 2016

ISSN: 2189-7948

DOI: 10.14442/jgfm.17.3_232