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題 名 | Sclerosing Perineurioma--A Case Report=硬化性神經束膜瘤--病例報告 |
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作 者 | 魏麗婷; 何信君; 曾興隆; | 書刊名 | 中華皮膚科醫學雜誌 |
卷 期 | 19:2 2001.06[民90.06] |
頁 次 | 頁112-116 |
分類號 | 415.827 |
關鍵詞 | 硬化性神經束膜瘤; Perineurioma; Epithelial membrane antigen; |
語 文 | 英文(English) |
中文摘要 | 神經束膜瘤包含數類變型屬於一種罕見之腫瘤,其組成細胞有特殊免疫化學及超微結構表現。從1978年Trombetta報告以來,神經束膜瘤被分為神經內〈又稱局部性肥厚性神經病變〉及神經外〈軟組織神經束膜瘤〉兩類。硬化性神經束膜瘤在1997年被提出,其特色為緻密組織、束狀或漩渦狀細胞分布與好發於年輕男性之手掌或手指。組成細胞亦有典型神經束膜細胞之免疫化學及超微結構表現。吾人報告一病例並討論相關文獻。 |
英文摘要 | Perinerurioma is a rare tumors with several variants. The composing cells have distinctive immunohistochemical and ultrastructural features of normal perineurial cells. Since Trombetta’s first description in 1978, perineurioma had been classified as intraneural (hypertrophic interstitial neuritis) and extraneural (soft tissue perineurioma) variants. In 1997, a new variant, sclerosing perineurioma, was described and was recognized by compact sclerosis, corded and whorled growth pattern and characteristic locations on the fingers or palms of young adults. The cells of sclerosing perineurioma show features of normal perineurial cells. Herein, we report on a case and review the related literature. |
本系統中英文摘要資訊取自各篇刊載內容。