神经甜味综合征:诊断难题。

IF 0.9 Q4 CLINICAL NEUROLOGY Neurohospitalist Pub Date : 2023-10-01 Epub Date: 2023-05-10 DOI:10.1177/19418744231174949
Karlos Acurio, Miguel Chuquilin
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引用次数: 0

摘要

Sweet综合征表现为急性发热、白细胞增多和特征性皮肤斑块。它可能涉及许多器官系统,但很少影响神经系统。我们报告一例51岁女性,表现为发烧、皮疹、头痛和脑病。脑磁共振成像显示广泛的T2高信号,涉及大脑半球、小脑和脑干。皮肤活检显示中性粒细胞浸润与Sweet综合征一致。她开始接受类固醇治疗,临床反应良好。进一步的询问显示,她在10年前也有类似的发作,被诊断为急性播散性脑脊髓炎。Neuro-Sweet综合征可能会出现一系列症状,并在很长一段时间内复发,这使得诊断变得困难而没有高度怀疑。临床医生应在急性脑炎伴有白质病变时考虑这种综合征,这些病变对类固醇反应强烈,尤其是在以前有类似症状的情况下。
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Neuro-Sweet Syndrome: A Diagnostic Conundrum.

Sweet Syndrome presents as acute fever, leucocytosis and characteristic skin plaques. It can involve many organ systems but rarely affects the nervous system. We report the case of a 51-year-old female that presented with fever, rash, headache and encephalopathy. Brain magnetic resonance imaging showed extensive T2 hyperintensities involving cerebral hemispheres, cerebellum, and brainstem. A skin biopsy revealed dermal infiltration by neutrophils consistent with Sweet Syndrome. She started steroid treatment with a good clinical response. Further questioning revealed that she had a similar episode 10 years prior that had been diagnosed as acute disseminated encephalomyelitis. Neuro-Sweet Syndrome can present with a great array of symptoms and relapses over long periods of time making the diagnosis difficult without a high degree of suspicion. Clinicians should consider this syndrome in the setting of acute encephalitis with white matter lesions that are highly responsive to steroids particularly in the presence of previous similar symptoms.

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来源期刊
Neurohospitalist
Neurohospitalist CLINICAL NEUROLOGY-
CiteScore
1.60
自引率
0.00%
发文量
108
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