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題 名 | Albright氏遺傳性骨發育不全症併原發性皮膚骨化=Primary Cutaneous Ossification in Albright's Hereditary Osteodystrophy |
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作 者 | 蕭中琦; 李俊諒; | 書刊名 | 中華皮膚科醫學雜誌 |
卷 期 | 17:1 1999.03[民88.03] |
頁 次 | 頁31-37 |
分類號 | 415.763 |
關鍵詞 | Albright氏遺傳性骨發育不全症; 原發性皮膚骨化; Albright's hereditary osteodystrophy; Pseudohypoparathyroidism; Pseudopseudohypoparathyroidism; Primary cutaneous ossification; |
語 文 | 中文(Chinese) |
英文摘要 | 原發性皮膚骨化發生在嬰孩是相當少見,Albright氏遺傳性骨發育不全症是可能 的原因之一。本例報告一位兩歲男孩自其一個月大時,四肢及腹部皮膚陸續出現硬塊,病理 切片檢查顯示真皮層存在異位性骨骼組織。患童外觀上具有肥胖、圓臉、智能不足等特徵, 並且手部X-ray檢查顯示表層軟組織鈣化及第四、五的掌骨生長板提早癒合之現象,其血液中 鈣、磷及副甲狀腺素皆在正常範圍內,根據以上特徵診斷為Albright氏遺傳性骨發育不全症 。 n phsical examination the child was characterized by obesity, round face and mental retardation. Radiography of the hands revealed early fusion of the growth plates of the 4th and 5th metacarpal bones. The serum calcium, phosphate, and parathyroid hormone levels were all within normal limits. He was diagnosed as Albright's hereditary osteodystrophy. |
本系統中英文摘要資訊取自各篇刊載內容。