頁籤選單縮合
題名 | mcindoe Vaginoplasty for the Treatment of Congenital Absence of Vagina: Experiences in Tri-Servie General Hospital=先天性無陰道症患者之陰道成形術治療 |
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作者 | 劉世明; 余慕賢; 尹長生; | 書刊名 | 醫學研究 |
卷期 | 17:3 1996.11[民85.11] |
頁次 | 頁181-186 |
分類號 | 417.153 |
關鍵詞 | 陰道成形術; Mayer-hauser-rokitansky症候群; Vaginoplasty; Mayer-hauser-rokitansky syndrome; |
語文 | 英文(English) |
英文摘要 | Congenital absence of vagina is a rare occurrence with an incidence of about 1/4,000 to 1/10,000. Most cases are resulted from aplasia of the Mullerian ducts known as Mayer-Rokitansky syndrome. It is often associated with congenital anomalies of urinary and skeletal systems. The most common treatment for this syndrome is reconstruction of neovagina by McIndoe operation. We have collected six patients of Mayer-Rokitansky syndrome in last ten years. The mean age of proved diagnosis was 17.8 (16 to 20) years old. Five of them were married and received reconstruction of neovagina by McIndoe operation. The mean age at operation was 24 (17 to 33) years old. The materials used for covering the neovagina were split-thickness skin graft (STSG) in three cases and amniotic membranes in two cases. Both grafted materials grew successfully without complication. After post-operative continuous dilatation and long-term follow-up, functional and anatomical results are satisfactory in both groups. This report is to review the reconstruction surgery of Mayer-Rokitansky syndrome and to analyze cases at our hospital. |
本系統之摘要資訊系依該期刊論文摘要之資訊為主。