P0705 / #733: SUCCESSFUL APPLICATION OF SYNTHETIC AND BIOLOGICAL SKIN SUBSTITUTE TO A CHILD WITH TOXIC EPIDERMAL NECROLYSIS

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منابع مشابه

Biological skin substitutes to treat toxic epidermal necrolysis in a case with human immunodeficiency virus infection

Toxic epidermal necrolysis (TEN) is a rare, but life-threatening medical emergency with significant morbidity and mortality. Current treatment standards for TEN patients include stopping all possible drugs associated with the new onset of symptoms, prompt referral and treatment in a specialized center with fluid resuscitation, adequate analgesia and maintenance of nutritional needs. Extensive d...

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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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Toxic epidermal necrolysis induced by lamotrigine treatment in a child

Toxic epidermal necrolysis is an unpredictable and severe adverse drug reaction. In toxic epidermal necrolysis, epidermal damage appears to result from keratinocyte apoptosis. This condition is triggered by many factors, principally drugs such as antiepileptic medications, antibiotics (particularly sulfonamide), nonsteroidal anti-inflammatory drugs, allopurinol, and nevirapine. Lamotrigine has ...

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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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ژورنال

عنوان ژورنال: Pediatric Critical Care Medicine

سال: 2021

ISSN: 1529-7535

DOI: 10.1097/01.pcc.0000741156.46986.a7