Abstract:
:Acute febrile neutrophilic dermatosis (Sweet syndrome) is rare in children and is regularly associated with underlying malignancies or inflammtory diseases. A 5-year-old girl with glycogen storage disease type Ib, neutropenia, and recurrent infections developed characteristic skin eruption of Sweet syndrome after 2 years of granulocyte colony-stimulating factor (G-CSF) therapy. This association points to a possible role of G-CSF-induced granulopoiesis and granulodyte activation in the pathogenesis of Sweet syndrome.
journal_name
Pediatricsjournal_title
Pediatricsauthors
Garty BZ,Levy I,Nitzan M,Barak Ysubject
Has Abstractpub_date
1996-03-01 00:00:00pages
401-3issue
3eissn
0031-4005issn
1098-4275journal_volume
97pub_type
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