Pediatric Sweet Syndrome: Case Report and Literature Review

被引：28

作者：

Halpern, James ^{[1
]}

Salim, Asad ^{[2
]}

机构：

[1] Univ Hosp N Staffordshire, Dept Dermatol, Cent Outpatients Dept, Stoke On Trent ST4 7PA, Staffs, England

[2] Mid Staffordshire Gen Hosp NHS Trust, Dept Dermatol, Stafford, England

来源：

PEDIATRIC DERMATOLOGY | 2009年 / 26卷 / 04期

关键词：

FEBRILE NEUTROPHILIC DERMATOSIS; CHRONIC GRANULOMATOUS-DISEASE; MULTIFOCAL OSTEOMYELITIS; INITIAL PRESENTATION; PUSTULAR VASCULITIS; RETINOIC ACID; DORSAL HANDS; CHILD; MALIGNANCY; MANIFESTATION;

D O I：

10.1111/j.1525-1470.2009.00952.x

中图分类号：

R75 [皮肤病学与性病学];

学科分类号：

100206 ;

摘要：

We report on an 18-month-old boy with a typical presentation of Sweet syndrome following an upper respiratory tract illness. No evidence of hematologic malignancy was found and he was successfully treated with oral prednisolone. A comprehensive literature review has summarized the features of pediatric Sweet syndrome from 66 reported cases. Cases occurring under the age of 3 years had a male predominance and no association with malignancy, whereas cases over the age of 3 years had an equal sex distribution and were strongly associated with myeloid line hematologic malignancies. Identified complications were serious with an overall mortality of 9% rising to 40% with cardiovascular involvement.

引用

页码：452 / 457

页数：6

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