Sedel D, Huguet P, Lebbe C, Donadieu J, Odièvre M, Labrune P
Service de Pédiatrie, Hôpital Antoine Béclère, Clamart, France.
Pediatr Dermatol. 1994 Sep;11(3):237-40. doi: 10.1111/j.1525-1470.1994.tb00593.x.
A 2.5-month-old infant had Sweet syndrome. Chronic granulomatous disease was subsequently diagnosed by the nitroblue tetrazolium reduction test. To date, this infant is the youngest reported with Sweet syndrome. Moreover, the association of chronic granulomatous disease with this syndrome has not been previously described. The precise relationship between the conditions remains to be determined. Granulocyte function should be evaluated in any infant with Sweet syndrome.
一名2.5个月大的婴儿患有Sweet综合征。随后通过硝基蓝四唑还原试验诊断出慢性肉芽肿病。迄今为止，该婴儿是报道中患有Sweet综合征最年幼的病例。此外，慢性肉芽肿病与该综合征的关联此前尚未有过描述。这两种病症之间的确切关系仍有待确定。对于任何患有Sweet综合征的婴儿，都应评估粒细胞功能。
