頁籤選單縮合
題名 | Pachydermoperiostosis--A Case Report=厚皮性骨膜病 |
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作者 | 蔡宜政; 全鳴鐸; 吳毅穎; | 書刊名 | 中華皮膚科醫學雜誌 |
卷期 | 18:2 2000.06[民89.06] |
頁次 | 頁156-162 |
分類號 | 416.674 |
關鍵詞 | 完全型厚皮性骨膜病; Pachydermoperiostosis; Complete form; |
語文 | 英文(English) |
中文摘要 | 厚皮性骨膜病為一罕見疾病,臨床上極似續發性肥大骨關節炎或肢端肥大症。一位二十二歲男性患者自十三歲開始出現杵狀指(趾)、厚皮以及四肢變粗。其長骨之放射線檢查呈現骨膜增生現象。額頭處之病理變化則呈現毛囊與皮脂腺肥大以及真皮、皮下組織之膠原束增厚現象。在徹底排除潛在性疾病及內分泌問題後,我們診斷此病例為完全型厚皮性骨膜病。 |
英文摘要 | Pachydermoperiostosis (PDP) is a rare disease that may mimic secondary hypertrophic osteoarhropathy or acromegaly. A 22-year-old man has been developing clubbing of fingers and toes, pachydermia, and enlargement of extremities since he was 13 years old. Roentgenograms of the long bones revealed a periosteal reaction. Histopatholgy of the skin from the forehead revealed hypertrophic pilosebaceous units and thickening collagen bundles in the dermis and subcutis. After extensive investigation excluding systemic or endocrine causes, we diagnosed it as a complete form of pachydermoperiostosis . |
本系統之摘要資訊系依該期刊論文摘要之資訊為主。