Giant cellulitis-like Sweet syndrome: An underrecognized clinical variant mimicking skin and soft tissue infection

被引:6
|
作者
Mitaka, Hayato [1 ]
Jammal, Rita [1 ]
Saabiye, Joseph [1 ]
Yancovitz, Stanley [1 ]
Perlman, David C. [1 ]
机构
[1] Icahn Sch Med Mt Sinai, Dept Med, Mt Sinai Beth Israel, First Ave & 16th St,Baird Hall 20th Floor, New York, NY 10003 USA
来源
IDCASES | 2020年 / 21卷
关键词
Giant cellulitis-like sweet syndrome; Acute febrile neutrophilic dermatosis; Cellulitis; Erysipelas; Skin and soft tissue infection;
D O I
10.1016/j.idcr.2020.e00874
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
A new clinical variant of Sweet syndrome, called giant cellulitis-like Sweet syndrome, can masquerade as cellulitis because the patients present with an acute onset of large erythematous plaques, fever, and leukocytosis with neutrophil predominance. This case describes a 90-year-old female with a history of invasive ductal carcinoma of the breast who presented with 3 days of erythema of the right chest and right leg. Physical examination was notable for well-demarcated, blanching erythematous rashes involving the right chest and right lower extremity. Laboratory data was notable for neutrophilic leukocytosis. A clinical diagnosis of cellulitis was made initially, and intravenous cefazolin was initiated. The rash had only partially improved with antibiotics. Skin biopsy revealed a dense neutrophilic infiltrate, which was consistent with Sweet syndrome. Based on the widespread plaques, this case was considered a "giant cellulitis-like" variant of Sweet syndrome. Clinicians should have a high index of suspicion for Sweet syndrome when assessing a patient with fever, neutrophilia and erythematous skin plaques atypical of cellulitis because this condition does not respond to antimicrobial therapy and requires systemic glucocorticoid therapy. (C) 2020 The Author(s). Published by Elsevier Ltd.
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