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以巨型口腔潰瘍表現的青少年型貝歇氏病合併壞死性血管炎-病例報告

A Juvenile Behçet's Disease Associated with Necrotizing Vasculitis Presenting by a Huge Oral Ulcer-A Case Report

摘要


貝歇氏病是一種全身性血管炎的疾病,其病灶通常表現在皮膚黏膜、眼睛及腸胃道,亦可能侵犯其他器官包括關節、中樞神經系統及所有血管。雖然該疾病的早期症狀偶有出現在16歲以前,但確診病例則較少出現在孩童時期。在此我們提出一個較少見的青少年型貝歇氏病,記錄其病程及治療過程,供研究及治療的參考。

並列摘要


Behçet's disease (BD) is a systemic vasculitis that commonly manifests itself in the form of mucocutaneous lesions, ocular and gastrointestinal involvements. It may also involve all organs such as the joints, central nervous system, and blood vessels of all types. The disease is uncommon in childhood, though it may occasionally present early onset before the age of 16 years. We report a rare juvenile Behçet's disease (JBD) and treatment course for the basis of further study.

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