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| 題 名 | Cranio-Facial Eosinophilic Granuloma--Case Report=嗜伊紅性肉芽腫--病例報告 |
|---|---|
| 作 者 | 龔蘭玉; 蕭弘道; | 書刊名 | 中華民國重建整形外科醫學會雜誌 |
| 卷 期 | 7:1 1998.03[民87.03] |
| 頁 次 | 頁68-72 |
| 分類號 | 415.132 |
| 關鍵詞 | Eosinophilic granuloma; Benign osteolytic lesion; |
| 語 文 | 英文(English) |
| 中文摘要 | 嗜伊紅性肉芽腫是以前被稱為「組織細胞增多症X」的蘭格罕細胞增多症候群的 一種,它以年輕人或孩童 ( 特別是男生 ) 的扁平骨內單一的或多發的骨質融解病害為代表 症狀。它是一種罕見而有較佳預後的良性本質的疾病。一個患有眼上眶緣嗜伊紅性肉芽腫的 五歲男孩在接受切除手術和術後局部放射治療後得到痊癒。從一九八八年到一九九五年裡馬 偕醫院共有五個嗜伊紅性肉芽腫病例在逆行性研究裡也被發現有不錯的預後 |
| 英文摘要 | Eosinophilic granuloma is one of the complex of Langerhans cell histiocytosis which was previously known as"Histiocytosis X". It is represented by unifocal or multifocal osteolytic lesion that occurs in flat bone of children and young adults,especially in males. It is a rare disorder but benign in nature with favorable prognosis. This paper describrd a 5 year old boy with supraorbital rim eosinophilic granuloma who treated with excision and local low dose postoperstive radiotherapy. The retrospective sudy of 5 cases of Mackay Memorial Hospital from 1988 to 1995was also reviewed. |
本系統中英文摘要資訊取自各篇刊載內容。