DRESS综合征(药物性皮疹伴嗜酸性粒细胞增多和全身症状):有时,并非所有症状都有

IF 0.3 Q3 MEDICINE, GENERAL & INTERNAL
Fábio Murteira, Pedro Oliveira, J. Miranda, A. Moreira, Margarida Correira
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引用次数: 1

摘要

DRESS综合征是一种罕见且可能致命的多系统反应,发生在接触某些药物后2至6周。它的特点是发热、嗜酸性粒细胞增多和皮疹。37岁男性,黑人,痛风(4周前开始使用别嘌呤醇)。他来到急诊室,主诉头痛、发烧、腹痛和分散的黄斑丘疹性皮肤病变。所进行的研究显示转氨酶和c反应蛋白升高,肝肿大和肝周围腺肿大。停用别嘌呤醇,但在整个住院期间,肝、肾和神经功能障碍(伴有脑膜脑炎)恶化;它还出现嗜酸性粒细胞增多。进行皮肤活检,假设有DRESS综合征的可能性,并开始使用甲基强的松龙2mg /kg/天,病情逐渐好转。皮肤活检符合DRESS。所描述的案例揭示了一些特点。其中最相关的是嗜酸性粒细胞的晚发性和由于患者的肤色和神经系统表现而难以评估皮疹(罕见)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
DRESS syndrome (drug rash with eosinophilia and systemic symptoms): sometimes, not all signs are there
DRESS syndrome is a rare and potentially fatal multisystemic reaction that occurs two to six weeks after exposure to certain drugs. It is characterized by fever, eosinophilia, and skin rash. Case of a 37-year-old man, black, with gout (started allopurinol 4 weeks before). He arrived at the Emergency Room complaining of headache, fever, abdominal pain, and scattered maculopapular skin lesions. The conducted study showed elevated transaminases and C-reactive protein, hepatomegaly, and peri-hepatic adenomegalies. Allopurinol was stopped, but throughout hospitalization, liver, renal and neurological dysfunctions (with meningoencephalitis) worsened; it also appeared eosinophilia. A skin biopsy was performed, the possibility of DRESS syndrome was assumed, and methylprednisolone 2 mg/kg/day was started, with progressive improvement. The skin biopsy was compatible with DRESS. The described case reveals some peculiarities. Among the most relevant arethe late onset of eosinophilia and the difficulty in evaluating the rash due to the patient's skin tone and neurological manifestations (rare).
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来源期刊
Italian Journal of Medicine
Italian Journal of Medicine MEDICINE, GENERAL & INTERNAL-
CiteScore
0.90
自引率
0.00%
发文量
3
审稿时长
10 weeks
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