Radhakrishna Veerbhadra, Govindarajan Krishna Kumar, Sambandan Kumaravel, Jindal Bibekanand, Naredi BikashKumar
Jawaharlal Institute of Postgraduate Medical Education & Research, Department of Pediatric Surgery, Pondicherry, 605006, India.
J Bras Nefrol. 2018 Jul-Sep;40(3):261-265. doi: 10.1590/1678-4685-jbn-3942. Epub 2018 Jun 18.
Children with solitary functioning kidney (SFK) are prone to develop long term problems, which are not well represented in the literature. The extent to which the presence of associated congenital anomalies of kidney and urinary tract (CAKUT) further de-stabilize renal function is to be addressed.
This study was conducted to evaluate the etiology, presentation, presence of CAKUT, and renal damage in children with SFK.
All children with SFK who presented to the department of pediatric surgery from March 2014 to May 2016 were included in the study. Children with malignancy were excluded from the study.
Of the 20 patients with SFK, 14 (70%) had primary SFK (8 with agenesis and 6 with multicystic dysplastic kidney), 6 (30%) belonged to secondary SFK group, among them 3 had pelviureteric junction obstruction, 2 had posterior urethral valves and 1 had vesicoureteric reflux. Eight (40%) had associated CAKUT, 4 (20%) were asymptomatic while 8 (40%) had UTI and 6 (30%) had hypertension. Ten (50%) patients had reduced glomerular filtration rate (GFR) suggesting compromised renal function.
Children with SFK have high morbidity especially when associated with ipsilateral CAKUT. Long-term periodical follow up is essential in these patients to improve clinical outcome.
患有孤立性功能肾(SFK)的儿童容易出现长期问题,而这些问题在文献中并未得到充分体现。肾脏和尿路相关先天性异常(CAKUT)的存在在多大程度上会进一步破坏肾功能,这一问题有待探讨。
本研究旨在评估患有SFK的儿童的病因、临床表现、CAKUT的存在情况以及肾脏损害情况。
纳入2014年3月至2016年5月期间到小儿外科就诊的所有患有SFK的儿童。患有恶性肿瘤的儿童被排除在研究之外。
在20例患有SFK的患者中,14例(70%)为原发性SFK(8例为肾缺如,6例为多囊性发育不良肾),6例(30%)属于继发性SFK组,其中3例有肾盂输尿管连接部梗阻,2例有后尿道瓣膜,1例有膀胱输尿管反流。8例(40%)伴有CAKUT,4例(20%)无症状,8例(40%)有尿路感染,6例(30%)有高血压。10例(50%)患者的肾小球滤过率(GFR)降低,提示肾功能受损。
患有SFK的儿童发病率较高,尤其是伴有同侧CAKUT时。对这些患者进行长期定期随访对于改善临床结局至关重要。