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題 名 | Idiopathic Multicentric Osteolysis: Report of an Affected Father and Son=特異多發性溶骨症:兩病例(父與子)報告 |
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作 者 | 刁偉民; 葉力仁; 馬景先; 潘慧本; 陳坤煌; | 書刊名 | 中華放射線醫學雜誌 |
卷 期 | 25:2 2000.04[民89.04] |
頁 次 | 頁91-95 |
分類號 | 416.26 |
關鍵詞 | 溶骨; 骨骼磁振造影; 家族性; 腕; Osteolysis; Bones MR; Familial conditions; Wrist; |
語 文 | 英文(English) |
中文摘要 | 特異多發性溶骨症是一罕見疾病。其特徵為漸進且廣泛的溶骨變化,最常從腕骨及附骨開始發生,通常沒有炎症反應伴隨。其病因不明,但其遺傳方式及是否伴有腎疾患則呈多元性的組合。我們報告一個罹患此症的四代家族中的一對父子,其臨床及放射學表徵符合此症之診斷,並簡要回顧相關文獻報導。因為此病的遺傳性及可能合併的致合腎疾,認識此病的典型臨床及放射學表徵益形重要。 |
英文摘要 | Idiopathic multicentric osteolysis is a rare disorder characterized by progressive and extensive bone loss, most frequently occuring in the carpal and tarsal areas, without clinical or laboratory evidence of inflammation. The etiology is unknown. The mode of genetic transmission in idiopathic multicentric osteolysis and its association with nephropathy are variable. We report a son and his father with typical radiological and clinical features of this disorder with progressive osteolysis of the carpal and tarsal bones. The disorder affects six members in this four-generation family. Recognition of this rare disorder and the unique radiological and clinical features is important not only because idiopathic multicentric osteolysis is a hereditary disease, but also due to its associated fatal nephropathy. We also briefly review the literature. |
本系統中英文摘要資訊取自各篇刊載內容。