Suppr超能文献

成人斯蒂尔病中的持久性斑块和线状色素沉着。

Persistent plaques and linear pigmentation in adult-onset Still's disease.

作者信息

Suzuki K, Kimura Y, Aoki M, Takezaki S, Tuchida T, Takano T, Kawana S

机构信息

Department of Dermatology, Nippon Medical School, Tokyo, Japan.

出版信息

Dermatology. 2001;202(4):333-5. doi: 10.1159/000051669.

Abstract

A 25-year-old Japanese man presented with high spiking fever, arthralgia and a skin rash. A pruritic edematous erythema with persistent plaques was found mainly on the trunk; these lesions persisted even when the fever subsided, with prominent linear pigmentation. As marked neutrophilia and a high level of serum ferritin were detected, a diagnosis of adult-onset Still's disease (AOSD) was made, even though the persistent eruption was not characteristic of the disease. Oral prednisolone, together with low-dose methotrexate, was given with good results. In the literature, a similar atypical rash has been reported in 11 cases in Japan. All of them required high-dose administration of corticosteroids or other immunosuppressive agents. Severe systemic complications were seen in 3 patients, and 2 cases died of the disease. Persistent plaques and linear pigmentation are some of the manifestations of AOSD, which cannot be overlooked. This appearance could be an indication that suggests an increased risk of systemic complications and a prolonged time to clinical remission.

摘要

一名25岁的日本男性出现高热、关节痛和皮疹。主要在躯干发现了伴有持续斑块的瘙痒性水肿性红斑;即使发热消退,这些皮损仍持续存在,并伴有明显的线状色素沉着。由于检测到明显的中性粒细胞增多和高水平的血清铁蛋白,尽管持续性皮疹并非该病的典型特征,但仍诊断为成人斯蒂尔病(AOSD)。给予口服泼尼松龙及小剂量甲氨蝶呤,效果良好。在文献中,日本有11例报告了类似的非典型皮疹。所有这些病例都需要大剂量使用皮质类固醇或其他免疫抑制剂。3例患者出现严重的全身并发症,2例死于该病。持续性斑块和线状色素沉着是AOSD的一些表现,不容忽视。这种表现可能提示全身并发症风险增加和临床缓解时间延长。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验