Sweet syndrome (SS) is a reactive neutrophilic process characterized by tender, erythematous papules and plaques, fever, and leukocytosis and is associated with underlying infections, inflammatory diseases, and malignant neoplasms. To our knowledge, only 2 cases of SS associated with new-onset systemic lupus erythematosus (SLE) have been reported—one in an adult woman and the other in a 14-year-old girl.1,2 We report the first case in an adult man.
Fernandes NF, Castelo-Soccio L, Kim EJ, Werth VP. Sweet Syndrome Associated With New-Onset Systemic Lupus Erythematosus in a 25-Year-Old Man. Arch Dermatol. 2009;145(5):608–609. doi:10.1001/archdermatol.2009.82
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