頁籤選單縮合
題名 | Left Multicystic Dysplastic Kidney with Contralateral Ureteropelvic Obstruction: Report of One Case=左側多囊性發育不良腎臟(MCDK)合併對側輸尿管腎盂阻塞: 一病例報告 |
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作者姓名(中文) | 翁根本; 邱益煊; 黃原逸; 宋秉洸; 謝凱生; 鍾全生; | 書刊名 | 中華民國小兒科醫學會雜誌 |
卷期 | 39:5 民87.09-10 |
頁次 | 頁339-341 |
分類號 | 417.574 |
關鍵詞 | 多囊性發育不良腎臟; 輸尿管腎盂阻塞; Multicystic dysplastic kidney; Ureteropelvic obstruction; Anuria; |
語文 | 英文(English) |
中文摘要 | 多囊性發育不良腎臟(MCDK)是新生兒常見的腹部腫瘤之一,這種疾病可合併對側 腎臟異常,如輸尿管腎盂阻塞等,由於多囊性發育不良腎臟(MCDK)是沒有功能的,仔細評估 對側腎臟情況就非常重要,如果對側腎臟有嚴重性阻塞就應立即治療,以保持腎功能,並避 免危及生命,我們報告一新生兒病例,產前即知有左側囊狀腎和右側水腎,產後24小時仍呈 現無尿情況,經緊急檢查,證實是左側多囊性發育不良腎臟(MCDK)合併對側輸尿管腎盂連接 處阻塞,給予妥善治療後,才避免危及生命,特此提出報告,並回顧相關文獻。 |
英文摘要 | Multicystic dysplastic kidney (MCD K) is a common cause of abdominal mass in neonates. It is frequently associated with malformation of the contralateral kidney, such as ureteropelvic obstruction, etc. Because MCDK is usually functionless, it is important to evaluate the condition of the contralateral kidney. The presence of severe obstruction in the contralateral ureteropelvic junction is life-threatening and prompt treatment should be made to preserve the remaining renal function. We report on a neonate with left MCDK and contralateral ureteropelvic obstruction, presenting as anuria after birth, and also we review the literature. |
本系統之摘要資訊系依該期刊論文摘要之資訊為主。