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急性发热性嗜中性皮病(斯威特综合征)。

Acute febrile neutrophilic dermatosis (Sweet's syndrome).

作者信息

Rahav G, Moses A, Michaeli J

机构信息

Department of Internal Medicine, Hadassah University Hospital, Mount Scopus, Jerusalem, Israel.

出版信息

Cutis. 1989 Aug;44(2):157-9.

PMID:2758865
Abstract

We describe a patient who displayed the classic features of acute febrile neutrophilic dermatosis (Sweet's syndrome): sudden onset of erythematous plaques, fever, arthritis, and characteristic histologic findings. Unusual findings in her case were the localization of the lesions mainly on the legs, absence of leukocytosis and preceding illness, and marked neutrophilic infiltration in the subcutis. In addition, the fever and eruption subsided on the day the results of pathologic examination were available, making any treatment unnecessary. The short course of the disease in this patient suggests the possibility of postponing steroid treatment for one week in all patients with acute febrile neutrophilic dermatosis.

摘要

我们描述了一位表现出急性发热性嗜中性皮病(Sweet综合征)典型特征的患者:突然出现红斑性斑块、发热、关节炎及特征性组织学表现。该病例的不寻常之处在于,皮损主要局限于腿部,无白细胞增多及前驱疾病,且皮下有明显的嗜中性粒细胞浸润。此外,在病理检查结果出来当天,发热和皮疹就消退了,无需进行任何治疗。该患者病程较短,提示对于所有急性发热性嗜中性皮病患者,有可能将类固醇治疗推迟一周。

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