Sternberg Kevan, Greenfield Saul P, Williot Pierre, Wan Julian
Department of Pediatric Urology, Women and Children's Hospital of Buffalo and Department of Urology, State University of New York at Buffalo School of Medicine, Buffalo, New York 14222, USA.
J Urol. 2005 Oct;174(4 Pt 2):1711-4; discussion 1714. doi: 10.1097/01.ju.0000179537.36472.59.
The presentation and management of pediatric stone disease have changed due to early identification and treatment of congenital urological conditions, as well as technological advances. Therefore, we reviewed our 12-year experience.
A total of 123 patients with 158 stones presented from 1991 to 2003. The 46 boys and 77 girls were 8 months to 25 years old, including 5 boys (4%) younger than 3 years, 46 (37%) 4 to 12 years old and 72 (59%) older than 13 years. A 24-hour urine collection was done in 50 patients (41%) and serum chemistry studies were performed in 66 (54%).
The seasons of presentation were fall in 41% of cases, summer in 24%, spring in 22% and winter in 13%. Of the patients 94 (76%) had loin pain, 10 (8%) had urinary tract infections, 13 (11%) had a history urinary tract infection, 18 (15%) had gross hematuria, 14 (11%) had structural urological abnormalities and 7 (6%) had neurogenic bladder. Metabolic abnormalities were uncommon and included hypercalciuria in 12%, hyperoxaluria in 2% and cystinuria in 2%. A total of 57 patients (46%) passed the stones and 34 (28%) underwent extracorporeal shock wave lithotripsy, of whom 24 (71%) became stone-free. Ureteroscopy was performed in 10 patients (8%) 6 to 19 years old, percutaneous nephrostolithotomy was done in 4 (3%) and 4 (3%) underwent open surgery. Stone analysis showed calcium based in 88% of the cases, struvite in 7% and cystine in 5%.
The majority of patients had no congenital abnormalities. Early diagnosis of urological abnormalities and urinary infection, and appropriate management of neurogenic bladder may have reduced the incidence in those groups. Most stones are calcium based but occur in the absence of metabolic disturbances. More patients presented in the fall, perhaps reflecting the increased concentration of urine in the summer. Half of the patients passed the stones and shock wave lithotripsy was curative in most others. Ureteroscopy, percutaneous nephrostolithotomy and open surgery were rarely required.
由于先天性泌尿系统疾病的早期识别与治疗以及技术进步,小儿结石病的表现和治疗方式已发生改变。因此,我们回顾了我们12年的经验。
1991年至2003年期间,共有123例患者出现158颗结石。46名男孩和77名女孩年龄在8个月至25岁之间,其中5名男孩(4%)年龄小于3岁,46名(37%)年龄在4至12岁之间,72名(59%)年龄大于13岁。50例患者(41%)进行了24小时尿液收集,66例(54%)进行了血清化学研究。
发病季节中,41%的病例在秋季,24%在夏季,22%在春季,13%在冬季。94例患者(76%)有腰痛,10例(8%)有尿路感染,13例(11%)有尿路感染病史,18例(15%)有肉眼血尿,14例(11%)有泌尿系统结构异常,7例(6%)有神经源性膀胱。代谢异常并不常见,包括高钙尿症占12%,高草酸尿症占2%,胱氨酸尿症占2%。共有57例患者(46%)结石自行排出,34例(28%)接受了体外冲击波碎石术,其中24例(71%)结石排净。10例6至19岁的患者(8%)接受了输尿管镜检查,4例(3%)接受了经皮肾镜取石术,4例(3%)接受了开放手术。结石分析显示,88%的病例为钙结石,7%为鸟粪石,5%为胱氨酸结石。
大多数患者没有先天性异常。泌尿系统异常和尿路感染的早期诊断以及神经源性膀胱的适当管理可能降低了这些人群中的发病率。大多数结石为钙结石,但在没有代谢紊乱的情况下发生。更多患者在秋季发病,这可能反映了夏季尿液浓度增加。一半的患者结石自行排出,大多数其他患者冲击波碎石术有效。很少需要输尿管镜检查、经皮肾镜取石术和开放手术。