We present the first reported instance of transient dermatographism occurring within 18 hours after birth in an otherwise healthy term newborn. The infant's dermatographism resolved without intervention or sequelae, and this report provides guidance for the clinician to follow when presented with similar presentations.
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http://dx.doi.org/10.1111/j.1525-1470.2007.00606.x | DOI Listing |
Pediatr Dermatol
April 2008
Department of Pediatrics, 60th Medical Group, Travis AFB, California 94535, USA.
We present the first reported instance of transient dermatographism occurring within 18 hours after birth in an otherwise healthy term newborn. The infant's dermatographism resolved without intervention or sequelae, and this report provides guidance for the clinician to follow when presented with similar presentations.
View Article and Find Full Text PDFAm J Hematol
January 2005
Indiana Oncology-Hematology Consultants, Indianapolis, Indiana 46107, USA.
A 38-year-old male with progressive myeloproliferative variant of hypereosinophilic syndrome (HES) underwent allogeneic bone marrow transplantation from a matched unrelated donor. The preparative regimen consisted of TBI, cytarabine, and cyclophosphamide. The graft was T-cell-depleted.
View Article and Find Full Text PDFPediatr Dermatol
January 2005
Division of Pediatric Dermatology, Department of Pediatrics, British Columbia's Children's Hospital, Vancouver, British Columbia, Canada.
The characteristic rash of systemic juvenile idiopathic arthritis is a transient erythematous eruption associated with a quotidian spiking fever. Usually asymptomatic, it can be pruritic, with dermatographism at sites of scratching or pressure. An illness similar to this entity in adults is designated adult-onset Still disease.
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