Kumar Gurinder, Stern Jonathan, Leslie Stephen W.
St. Barnabas Hospital
Creighton University School of Medicine
Horseshoe kidney is the most common congenital renal fusion anomaly, with an incidence of approximately 1 in 500 live births. As first described in autopsy studies by da Carpi in 1522, a horseshoe kidney is characterized by the fusion of the lower poles of the kidneys across the midline. This anomaly is typically associated with vascular, rotational, and positional anatomical abnormalities, typically resulting in a U-shaped unitary renal unit configuration in the midabdomen, positioned lower in position than normal kidneys. The isthmus, which connects the 2 renal masses, typically (80%) consists of functioning renal parenchyma with its own blood supply, but it may also be composed of fibrous tissue. The connecting isthmus is located between the lower poles in over 90% of cases, but it may occur elsewhere in a small minority. The kidneys are malrotated, with their lower poles fused and their collecting systems facing anteriorly. As they descend to the bladder, the ureters pass anterior to the isthmus, typically located immediately below the inferior mesenteric artery. Abnormal courses of the ureters predispose them to ureteral obstruction and stasis. Horseshoe kidneys demonstrate a significant variation in the origin and number of renal arteries and veins. Vascularization is mainly dependent on where the renal ascent is terminated in development. In a study involving 90 horseshoe kidneys, 387 separate arteries were identified.Nevertheless, the regular intrarenal segmental, non-collateral arterial vascular pattern remains, and ligation or division of any renal arteries results in ischemic segmental renal ischemia or necrosis. The incidence of renal vein anomalies in horseshoe kidneys is also high at 23%. The natural history is generally benign; however, affected individuals are at increased risk for complications such as ureteropelvic junction obstruction, hydronephrosis, nephrolithiasis, urinary tract infections, vesicoureteral reflux, and renal malignancies, such as renal cell carcinoma, transitional cell cancer, and Wilms tumor in children. The overall risk of a renal malignancy in a horseshoe kidney is about 3 to 4 times higher than in the general population. There is also a higher risk of traumatic injury to the kidney due to its lower position, anterior location, and lack of protection from the rib cage, although such injuries are rarely reported. Chronic kidney disease and progression to end-stage renal disease are more common in this population, likely due to the high prevalence of associated genitourinary anomalies and complications. The abnormal vasculature and collecting system anatomy can complicate the presentation and management of disease, particularly surgical procedures. Extrarenal anomalies, including gastrointestinal and vertebral malformations, are also more frequent in affected individuals, especially in pediatric populations.
马蹄肾是最常见的先天性肾融合异常,活产儿中的发病率约为1/500。正如1522年达·卡尔皮在尸检研究中首次描述的那样,马蹄肾的特征是双肾下极在中线处融合。这种异常通常与血管、旋转和位置解剖异常有关,通常会在中腹部形成一个U形的单一肾单位结构,位置比正常肾脏更低。连接两个肾块的峡部通常(80%)由具有自身血液供应的功能性肾实质组成,但也可能由纤维组织构成。在超过90%的病例中,连接峡部位于下极之间,但在少数情况下也可能出现在其他部位。肾脏旋转异常,下极融合,集合系统向前。当它们下降至膀胱时,输尿管在峡部前方通过,峡部通常位于肠系膜下动脉下方紧邻处。输尿管走行异常使其易发生输尿管梗阻和淤积。马蹄肾的肾动脉和肾静脉在起源和数量上有很大差异。血管形成主要取决于肾脏在发育过程中上升终止的位置。在一项涉及90个马蹄肾的研究中,共识别出387条独立动脉。尽管如此,肾内节段性、无侧支动脉血管模式仍然存在,结扎或切断任何肾动脉都会导致节段性肾缺血或坏死。马蹄肾中肾静脉异常的发生率也较高,为23%。其自然病程通常是良性的;然而,患者发生诸如肾盂输尿管连接部梗阻、肾积水、肾结石、尿路感染、膀胱输尿管反流以及肾恶性肿瘤(如肾细胞癌、移行细胞癌和儿童肾母细胞瘤)等并发症的风险增加。马蹄肾发生肾恶性肿瘤的总体风险比普通人群高约3至4倍。由于其位置较低、位于前方且缺乏肋骨保护,肾脏遭受创伤性损伤的风险也较高,尽管此类损伤很少被报道。慢性肾脏病及进展至终末期肾病在该人群中更为常见,可能是由于相关泌尿生殖系统异常和并发症的高患病率。肾外异常,包括胃肠道和脊柱畸形,在患者中也更常见,尤其是在儿童人群中。