Delgado Martínez J R, Inglada Galiana L, Sánchez Hernández J A, Cabrera Galván J J, Hernández Hernández B, Amerigo García M J
Rev Clin Esp. 1989 Oct;185(5):246-9.
In 1964 Sweet described a new syndrome which was characterized by pyrexia, neutrophilia, and the abrupt appearance of erythematous, painful, cutaneous plaques, primarily on the upper extremities, head, and neck. Histologically, the prominent feature is a dense dermal infiltrate of neutrophils, without signs of vasculitis, with a prompt response to steroid therapy. Since then up to 150 cases have been reported, being actually considered an immune mechanism responsible of this syndrome and we now have criterions for the diagnosis of it. We report a patient with Sweet's syndrome (SS): who has all the diagnostic criterions, whose main interest is having suffered from erythema nodosum three years before; this is the second case we have found in the English literature, and we also discuss some peculiarities.
1964年，斯威特描述了一种新的综合征，其特征为发热、中性粒细胞增多，以及主要出现在上肢、头部和颈部的红斑性、疼痛性皮肤斑块突然出现。组织学上，突出特征是真皮内密集的中性粒细胞浸润，无血管炎迹象，对类固醇治疗反应迅速。从那时起，已报告了多达150例病例，实际上认为是该综合征的一种免疫机制，并且我们现在有了其诊断标准。我们报告了一名患有斯威特综合征（SS）的患者：该患者具备所有诊断标准，其主要关注点是三年前曾患结节性红斑；这是我们在英文文献中发现的第二例病例，并且我们还讨论了一些特殊情况。
