頁籤選單縮合
題名 | Congenital Multiple Plaque-Like Glomangiomyoma in Trunk--A Case Report=軀幹部先天多發性斑狀血管球肌瘤--病例報告 |
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作者 | 林才民; 蔡志成; 蔡坤寶; 賴春生; 林幸道; 吳明峰; Lin, Tsai-ming; Tsai, Chih-cheng; Tsai, Kun-bow; Lai, Chung-sheng; Lin, Sin-daw; Wu, Ming-fang; |
期刊 | The Kaohsiung Journal of Medical Sciences |
出版日期 | 20010700 |
卷期 | 17:7 2001.07[民90.07] |
頁次 | 頁377-380 |
分類號 | 415.38 |
語文 | eng |
關鍵詞 | 先天多發性斑狀血管球肌瘤; Congenital glomus tumor; Glomangiomyoma; Trunk; |
中文摘要 | 先天性血管球瘤是血管球瘤中罕見的變異; 而血管球肌瘤在組織學上 更是血管球瘤最少見的一種。我們提出一例11歲男孩右側軀幹的先天多發性斑 狀血管球肌瘤,組織病理學顯示典型血管球細胞逐漸轉移為平滑肌肉細胞。就文 獻查詢,本病例-軀幹部先天多發性斑狀血管球肌瘤是世界首例。 |
英文摘要 | Congenital glomus tumor is a rare variant of glomus tumor, and glomangiomyoma is the least frequent histological type of glomus tumor. We present a case of congenital multiple plaque-like glomangiomyoma in an 11-year-old child with multiple diffuse plaques on his right lateral trunk. Histopathologic study showed a picture of typical glomus cell undergoing transition to smooth muscle cell. After literature review, this might be the first case report of congenital multiple plaque-like glomus tumor in trunk with histological appearance of a glomangiomyoma. |
本系統之摘要資訊系依該期刊論文摘要之資訊為主。