Abstract
Histiocytoid Sweet's syndrome is a recently described entity which has clinical features identical to typical Sweet's syndrome but is distinguished by a dermal cellular infiltrate composed not of mature neutrophils but of immature granulocytes. Herein, we report a case of bone marrow granulocytic maturation arrest and a histological histiocytoid Sweet's-like reaction pattern following trimethoprim-sulfamethoxazole therapy. © Blackwell Munksgaard 2007.
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CITATION STYLE
Wu, A. J., Rodgers, T., & Fullen, D. R. (2008). Drug-associated histiocytoid Sweet’s syndrome: A true neutrophilic maturation arrest variant. Journal of Cutaneous Pathology, 35(2), 220–224. https://doi.org/10.1111/j.1600-0560.2007.00780.x
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