抗磷脂抗体阳性斯内登综合征:病例报告。

Q4 Dentistry Folia medica Pub Date : 2024-02-29 DOI:10.3897/folmed.66.e106231
Bünyamin Tosunoğlu, Fadima Serap Basut, Beyza Başer, Melih Altikardeş, Levent Ertuğrul Inan
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引用次数: 0

摘要

斯内登综合征可能会出现神经系统症状,如短暂性缺血性中风、脑卒中、癫痫发作和/或头痛。然而,在出现神经系统症状之前,皮肤上可能会出现一种紫红色、蜘蛛网状的皮肤症状,称为网状细胞增多症。斯内登综合征常累及女性。由于这是一种影响中小血管的血管病变,因此可能伴随其他器官的病变。我们为大家介绍一位 44 岁的斯内登综合征患者,她左下肢单瘫,背部和腿部出现活体网状结构,并伴有高血压。
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Antiphospholipid antibody positive Sneddon syndrome: a case report.

Sneddon syndrome may present with neurological findings such as transient ischemic stroke, strokes, seizures and/or headaches. However, a purplish, spider web-like skin finding called livedo reticularis may accompany the skin and precede neurological findings. Sneddon syndrome often affects women. Since it is vasculopathy affecting small and medium vessels, other organ findings may accompany. We present a 44-year-old Sneddon syndrome patient with monoparesis in her left lower extremity, livedo reticularis on her back and legs, and hypertension.

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来源期刊
Folia medica
Folia medica Medicine-Medicine (all)
CiteScore
1.00
自引率
0.00%
发文量
121
审稿时长
5 weeks
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