Stevens Johnson syndrome and toxic epidermal necrolysis at the Hospital Universitario del Valle “Evaristo García” for a period of 9 years.

Authors

  • David Andrés Arias
  • Paola Andrea Londoño
  • Juana Gabriela López
  • Luis Hernando Moreno

DOI:

https://doi.org/10.29176/2590843X.256

Keywords:

Stevens Johnson, syndrome, toxic epidermal necrolysis, tumor necrosis factor alpha, pentoxifylline

Abstract

The Stevens-Johnson syndrome and the toxic epidermal necrolysis are very severe cutaneous drug reactions and constitute a spectrum of the same disease, sharing etiological, pathogenic, histological and therapeutic aspects.
Objectives: To describe the cases of toxic epidermal necrolysis and Stevens-Johnson syndrome over a nine year period at the Hospital Universitario del Valle, the treatments used in these patients and their mortality.
Methodology: A medical history review was carried out retrospectively of patients with Stevens-Johnson syndrome and toxic epidermal necrolysis diagnosed and managed from February, 2003, until April, 2012, at the Hospital Universitario del Valle. We analyzed clinical characteristics, frequency, mortality, medications as possible triggers, treatments used and response to them.
Results: Out of 29 cases, 13 (44.8%) had diagnosis of toxic epidermal necrolysis, 13 (44.8%) had Stevens-Johnson syndrome and the remaining 3 (10.3%), overlapping Stevens-Johnson syndrome-toxic epidermal necrolysis. In 16 patients (55%) a single drug could be the trigger. In 12 patients (41%) two or more drugs were found as possible triggers. Drugs were identified only in one. Antibiotics, anticonvulsants, NSAIDs and allopurinol were the most frequently associated drugs. All patients received supporting measures. Twenty patients (68%) received antibiotic therapy due to an associated infection. Twenty three patients (79.3%) received pentoxifylline as part of their treatment; six (20.6%) received gammaglobulin (two of them associated with oral pentoxifylline). One patient died (3.4%).
Conclusions: The supporting measures are essential in the management of patients with toxic epidermal necrolysis and Stevens- Johnson syndrome independent of the affected body area, as well as the timely management of complications as superinfection. Pentoxifylline may be considered an alternative in the treatment of these pathologies.

Author Biographies

David Andrés Arias

Médico, residente de Dermatología y Cirugía Dermatológica, Universidad del Valle, Cali, Colombia.

Paola Andrea Londoño

Médica dermatóloga, Universidad del Valle, Cali, Colombia.

Juana Gabriela López

Médica dermatóloga, Universidad del Valle, Cali, Colombia.

Luis Hernando Moreno

Médico dermatólogo, M.Sc. en Microbiología; jefe, Departamento de Dermatología y Cirugía Dermatológica, Universidad del Valle, Cali, Colombia

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How to Cite

1.
Arias DA, Londoño PA, López JG, Moreno LH. Stevens Johnson syndrome and toxic epidermal necrolysis at the Hospital Universitario del Valle “Evaristo García” for a period of 9 years. rev. asoc. colomb. dermatol. cir. dematol. [Internet]. 2013 Jul. 1 [cited 2024 Jul. 3];21(3):214-9. Available from: https://revista.asocolderma.org.co/index.php/asocolderma/article/view/256

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Published

2013-07-01

How to Cite

1.
Arias DA, Londoño PA, López JG, Moreno LH. Stevens Johnson syndrome and toxic epidermal necrolysis at the Hospital Universitario del Valle “Evaristo García” for a period of 9 years. rev. asoc. colomb. dermatol. cir. dematol. [Internet]. 2013 Jul. 1 [cited 2024 Jul. 3];21(3):214-9. Available from: https://revista.asocolderma.org.co/index.php/asocolderma/article/view/256

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