| Literature DB >> 30834560 |
Lana Chafranska1,2, Ditte M Saunte1,2, Nille Behrendt2,3, Ulrikka Nygaard4, Ryan J Christensen5, Carsten Sand6, Gregor B Jemec1,2.
Abstract
Successful management of toxic epidermal necrolysis (TEN) with tumor necrosis factor-α inhibitors has been described in adults. We present a case of a 7-year-old boy with infection-associated TEN, diagnosed by typical clinical and histopathological features, most likely caused by Mycoplasma pneumoniae. Treatment with a single dose of infliximab 5 mg/kg intravenously on day 5 after the onset of symptoms was followed by cessation of all blister formation over 3 days and complete resolution within a week. Sequelae were mild, consisting of postinflammatory hyperpigmentation and dry eyes.Entities:
Keywords: Stevens-Johnson syndrome; infliximab; mycoplasma pneumoniae; toxic epidermal necrolysis; toxic epidermal necrolysis, alpha inhibitor
Year: 2019 PMID: 30834560 DOI: 10.1111/pde.13778
Source DB: PubMed Journal: Pediatr Dermatol ISSN: 0736-8046 Impact factor: 1.588