- 期刊
Rhabdomyomatous Mesenchymal Hamartoma Associated with Congenital Anomalies: Report of an Unusual Perineal Case
橫紋肌間葉型錯構瘤伴隨先天異常：一個罕見的會陰部病例報告
摘要
橫紋肌異常的在皮膚出現是一個稀有的狀況。這樣的病灶目前被命名為橫紋肌間葉型錯構瘤，但因為橫紋肌並不屬於正常皮膚的成分，更正確的來說，他應該被命名為皮膚橫紋肌迷離瘤。我們提出一個發生在會陰部的病例，他同時合併了羊水帶症候群、無肛症及腸道閉鎖。伴隨著先天性腸胃道異常的情況以往並未曾被報告過。我們報告一個罕見的病例並且和另外兩個發生在會陰部的病例作比較。
關鍵字
無資料並列摘要
The ectopic occurrence of skeletal muscles in skin is an unusual condition. These lesions are named rhabdomyomatous mesenchymal hamartoma now. More accurately speaking, this entity should be called ”cutaneous rhabdomyomatous choristoma” because the skeletal muscle is not a normal element in skin. We described a case occurring in perineal region associated with amniotic band syndrome, imperforate anus, and intestinal atresia. The association with gastrointestinal tract anomaly has not been reported previously. This unusual case is documented and compared to two other cases reported in this region.
延伸閱讀
- Ng, H. C., & Lee, R. F. (1991). 疑先天性弓漿蟲視網膜脈絡膜炎―病例報告及文獻討論. 中華民國眼科醫學會雜誌, 30(1), 154-158. https://doi.org/10.30048/ACTASOS.199112.0027
- Lai, M. Y., & Tzung, T. Y. (2002). 先天性外胚層發育異常：兩則偶發性病例報告. 中華皮膚科醫學雜誌, 20(4), 308-312. https://www.airitilibrary.com/Article/Detail?DocID=10278117-200212-20-4-308-312-a
- Lee, H. C., Liang, H. H., Chai, C. Y., Tam, K. W., Chen, C. S., Wu, C. H., Wu, C. H., Chen, S. C., Chen, W. Y., & Lien, Y. C. (2008). 呈現前縱隔腔囊狀腫瘤之膈神經許旺氏細胞瘤：病例報告. Formosan Journal of Surgery, 41(5), 231-234. https://doi.org/10.29833/FJS.200810.0008
- Chang, C. J., & Yeh, M. L. (2004). 罕見的先天性橫膈疝氣：病例報告. Formosan Journal of Surgery, 37(5), 234-237. https://doi.org/10.29833/FJS.200410.0007
- 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