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| 題 名 | Silicosis Complication with Systemic Scleroderma with Interstitial Pneumonitis--Erasmus Syndrome=矽肺症併發全身性硬皮症合併間質性肺炎--伊拉斯謨綜合症 |
|---|---|
| 作 者 | 林昌生; | 書刊名 | 秀傳醫學雜誌 |
| 卷 期 | 23:3 2024.12[民113.12] |
| 頁 次 | 頁421-427 |
| 分類號 | 415.46 |
| 關鍵詞 | 系統性硬化症; 伊拉斯謨綜合症; 肺功能; 運動心肺功能測試; 開胸肺切片; 環磷醯胺; 腎上腺皮質酮; Systemic sclerosis; Erasmus syndrome; Pulmonary function test; Cardiopulmonary exercise testing; Open lung biopsy; Cyclophosphamide; Prednisolone; |
| 語 文 | 英文(English) |
| DOI | 10.30185/SCMJ.202412_23(3).0013 |
| 中文摘要 | 雖然嚴重的呼吸困難不常發生於單純性矽肺病患,但此症狀可能會隨著矽肺病或其他疾病所產生的肺部間質性纖維化而發生,例如系統性硬化症(硬皮症)。這篇文章描述了一位患有長期矽肺病的患者,突然出現呼吸困難症狀,繼而發現間質性肺炎和肋膜積水並伴隨有硬皮症的皮膚表現。經由肺灌洗和切片等檢查後,他接受了prednisolone和cyclophosphamide治療,顯著改善了他的肺功能和運動能力。此外,此篇還討論了此疾病的診斷及治療。 |
| 英文摘要 | Although severe dyspnea is uncommon in patients with simple silicosis, it may occur with pulmonary interstitial fibrosis caused by silicosis or other disorders such as systemic sclerosis (scleroderma). This article describes the case of a patient with long-standing silicosis who suddenly developed dyspnea and was subsequently diagnosed with interstitial pneumonitis, pleural effusion, and skin manifestations of scleroderma. After lung lavage and biopsy, the patient was treated with prednisolone and cyclophosphamide, which significantly improved their lung function and exercise capacity. This article also discusses the diagnosis and management of this condition. |
本系統中英文摘要資訊取自各篇刊載內容。