| Literature DB >> 30187958 |
Anna-Marie Hosking1, Joy Makdisi1, Francesca Ortenzio1, Sebastien de Feraudy1, Janellen Smith1, Kenneth Linden1.
Abstract
A 6-month-old boy was referred to our burn unit with a recurrent bullous dermatitis, fever, and emesis, originally diagnosed as staphylococcal scalded skin syndrome (SSSS) at an outside hospital. Infectious workup was negative and shave biopsy revealed a dense, diffuse dermal infiltrate of mast cells, consistent with diffuse cutaneous bullous mastocytosis-a rare variant of cutaneous mastocytosis. Treatment included a prolonged course of corticosteroids and antihistamines. Recognition of this rare form of mastocytosis is important, as it can be easily mistaken for other pediatric bullous diseases and is associated with life-threatening complications including vasodilation, anaphylactic shock, gastrointestinal bleeding, and death.Entities:
Keywords: mastocytosis; vesiculobullous disorders
Mesh:
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Year: 2018 PMID: 30187958 DOI: 10.1111/pde.13651
Source DB: PubMed Journal: Pediatr Dermatol ISSN: 0736-8046 Impact factor: 1.588