- 期刊
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
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。我們提出一列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。
關鍵字
無資料並列摘要
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.
延伸閱讀
- Chiau, J. H., Chang, T. K., Hwang, B., & Tiu, C. M. (1990). 胸骨嗜伊紅性肉芽腫：一病例報告. Acta Paediatrica Sinica, 31(1), 35-39. https://www.airitilibrary.com/Article/Detail?DocID=00016578-199002-31-1-35-39-a
- Sheen, J. M., Lee, Z. F., Hsu, C. H., & Lai, M. T. (2000). 先天性橫紋肌肉瘤－病例報告. The Kaohsiung Journal of Medical Sciences, 16(12), 634-637. https://doi.org/10.6452/KJMS.200012.0634
- Tsao, T. Y., Tseng, H. H., Shih, C. M., Nieh, S., & Tu, Y. C. (1991). 惡性神經髓鞘瘤合併橫紋肌胚瘤分化（惡性蠑螈瘤）：病例報告及文獻覆閱. Journal of Medical Sciences, 11(5), 389-399. https://www.airitilibrary.com/Article/Detail?DocID=10114564-199110-201307260006-201307260006-389-399
- Hsieh, T. J., Kuo, Y. T., Tsai, K. B., Hwang, S. L., Chou, M. S., Liu, G. C., & Wang, C. K. (2002). 頸椎硬腦膜外脈絡球血管瘤以啞鈴狀腫瘤表現─病例報告. The Kaohsiung Journal of Medical Sciences, 18(5), 253-256. https://doi.org/10.6452/KJMS.200205.0253
- 吳俊良、趙文元、黃澤人、曾惠仁、靳應台（1993）。顳骨橫紋肌肉瘤－病例報告。中華民國耳鼻喉科醫學會雜誌，28(4)，269-274。https://doi.org/10.6286/1993.28.4.269