Costigan Caoimhe S, Rosenblum Norman D
Division of Nephrology, The Hospital for Sick Children, Toronto, ON, Canada.
Developmental & Stem Cell Biology Program, Research Institute, The Hospital for Sick Children, Toronto, ON, Canada.
Front Urol. 2023 Apr 19;3:1154740. doi: 10.3389/fruro.2023.1154740. eCollection 2023.
Congenital anomalies of the urinary tract are a major cause of chronic kidney disease in both adults and children. Ureteropelvic junction obstruction, usually detected as urinary tract dilatation , is one of the most common forms of CAKUT. As antenatal ultrasound technology advances and screening becomes more widespread, increasing numbers of infants with this UPJO will be detected. Management of these infants presents a clinical conundrum, as distinguishing mild benign cases from those who may develop severe renal impairment is challenging. Herein we propose that an understanding of normal developmental and pathological mechanisms involved in UPJO is important in the armamentarium for tackling this challenging condition.
先天性泌尿系统异常是成人和儿童慢性肾脏病的主要原因。肾盂输尿管连接处梗阻通常表现为尿路扩张,是先天性肾脏和尿路畸形(CAKUT)最常见的形式之一。随着产前超声技术的进步和筛查的普及,越来越多患有这种肾盂输尿管连接处梗阻的婴儿将被检测出来。这些婴儿的治疗面临着临床难题,因为区分轻度良性病例和可能发展为严重肾功能损害的病例具有挑战性。在此,我们提出,了解肾盂输尿管连接处梗阻所涉及的正常发育和病理机制对于应对这一具有挑战性的病症至关重要。