Congenital solitary functioning kidney: evaluations to do which, when, and how

US has a low predictive value in low-grade VUR detection. This leads us to consider performing voiding cystourethrogram (VCUG) in patients with CSFK; however, whether it should be performed in all patients with CSFK is debatable. We examine for VUR not because we are concerned about the presence of VUR itself but because we are concerned about the damage to a solitary functioning kidney caused by urinary tract infection (UTI). If the evidence is clear that low-grade VUR is associated with a lower frequency of UTI and a lower likelihood of kidney scarring, and US is a fairly good indicator of high-grade VUR, we may only perform VCUG in patients with abnormal US findings. Some researchers have reported evidence of this. One study analyzed 156 patients with unilateral MCDK [ 24 ] and observed that only 1.7% of the patients with normal contralateral kidneys on US had high-grade VUR (grades 4–5), compared with 13.2% of those with abnormal US findings. This suggested that children with MCDK who have normal contralateral kidneys on US have a low incidence of clinically significant high-grade VUR. Moreover, they described the significant association between abnormal CSFK on US, including HN, duplex configuration, ureterocele, hydroureter, or uroepithelial thickening, and severe VUR. However, the only factor that was statistically significant in the comparison of patients with and without UTI was female gender, not VUR or abnormal US findings. Another study [ 25 ] described VUR in 77 children with MCDK examined using VCUG. The study showed no significant association between severe VUR and UTI and concluded that VCUG did not lead to changes in the management of the patients (e.g., antibiotic prophylaxis) before and after acquiring knowledge about the presence of VUR. However, due to the limited number of available studies and enrolled patients, the decision to perform VCUG is left to the opinion of the clinician.

To date, several recommendations on the type and timing of laboratory tests for patients with CSFK are available [ 9 , 14 , 27 - 30 ]. These papers do not recommend routine blood tests when CSFK has good compensatory growth; however, they have recommended urinalysis to examine for proteinuria at diagnosis. However, if the patient with CSFK has abnormal US findings or additional indications including obstructive uropathy, UTI, preterm birth, or low birth weight, they have recommended evaluating serum creatinine and quantifying proteinuria. This is because those with no additional CAKUT and sufficient compensatory growth were less likely to have high blood pressure, proteinuria, or decreased kidney function [ 9 , 27 , 28 ]. The published recommendations are summarized in Fig. 1 .

Among the CSFK-associated urologic abnormalities, vesicoureteral reflux (VUR) is the most common [ 2 , 3 , 9 , 16 , 24 ]. Previous studies on the prevalence of CSFK-associated CAKUT are summarized in Table 1 [ 14 ]. Among these studies, two systematic reviews analyzing large populations of patients with MCDK or URA were included [ 2 , 3 ]. In 2009, Schreuder et al. [ 2 ] conducted a meta-analysis of 67 cohort studies with more than 3,500 patients with MCDK. One-third of the patients with MCDK had a contralateral kidney anomaly, with VUR being the most common anomaly and accounting for 20% of the cases. Of the patients with VUR, 40% had high grades of over 3. Conversely, a meta-analysis of 43 studies with 2,684 patients with URA conducted by Westland et al. in 2013 [ 3 ] showed anomalies at the solitary kidney in approximately 30% of the patients, which is consistent with the results of previous meta-analyses on MCDK. VUR, accounting for 24%, was the most common urologic anomaly. However, the VUR grade was not analyzed in this study.

Genital malformations are more common in female patients with CSFK; however, they may be presented in ipsilateral seminal vesicle hypoplasia, absence of the vas deferens in males occasionally. Uterine vaginal agenesis, uterine duplicity, obstructive or blind hemivagina, monoliteral ovarian agenesis, and Gartner duct pseudocyst are the types of anomalies. Moreover, genital anomalies are frequently associated with various syndromes, including HWW/OHVIRA and MURCS syndrome. As previously described, up to 30% of patients with URA are associated with Müllerian anomalies. Conversely, more than 50% of patients with Müllerian anomalies and 92% to 100% of patients with obstructive hemivagina have kidney anomalies [ 31 - 33 ]. Uterine anomalies occur in one in over 500 females, 43% of whom have URA [ 34 ]. Although the kidney anomalies that are most commonly associated with Müllerian anomalies are URA and MCDK, unilateral or bilateral pelvic kidney, horseshoe kidney or kidney crossed ectopia, pyelocaliceal duplicity, ectopic ureter, and bilateral pyelectasis have also been reported [ 35 ]. Screening young women with URA and MCDK for Müllerian anomalies is significant owing to the potential for complications from untreated obstructive malformations [ 31 , 36 - 38 ]. Obstructive anomalies of the female genital tract can lead to retrograde menstruation, which develops significant problems including endometriosis, pelvic inflammatory disease, and infertility. However, prenatal US is unreliable for genital malformation screening, and several patients with obstructive genital anomalies can be asymptomatic during childhood. Therefore, when URA is identified in antenatal periods, physicians must explain to parents the significance of proper screening before menarche. To exclude genital abnormalities between thelarche and menarche, abdominopelvic US must be performed in all females with CSFK. Pelvic MRI is the gold standard of assessment; however, pelvic three-dimensional US may be an alternative for MRI [ 39 ]. Genital examination should include checking for a vaginal bulge or lower abdominal mass, indicating mucocolpos. Drainage of hematocolpos and vaginal septum excision comprise the treatments of obstructive genital malformations [ 37 ].

Literatures have suggested that approximately 30% of patients with CSFK have extrarenal malformations [ 2 , 3 , 7 , 9 , 10 ]. Extrarenal malformations can develop in the heart, gastrointestinal tract, musculoskeletal system, and genital tract. Regarding additional CAKUT in the contralateral kidney, the studies by Schreuder et al. [ 2 ] and Westland et al. [ 3 ] included the largest number of patients with CSFK and reported that approximately 15% and 31% of the patients with MCDK and URA have extrarenal manifestations, respectively, and up to 10% have syndromic features. The study by Schreuder also observed that up to 11% of female patients with URA have genital malformations, including obstructive hemivagina, uterine didelphys, and Müllerian duct aplasia-hypoplasia. The most reported syndromes are described in Table 2 . Among these syndromes, Herlyn–Werner–Wunderlich (HWW) or obstructive hemivagina and ipsilateral renal agenesis (OHVIRA) and Müllerian duct aplasia–renal agenesis-cervicothoracic somite dysplasia (MURCS) have CSFK with female genital malformations and autosomal dominant inheritance.

CSFK should be confirmed using neonatal US after birth when suspected prenatally because prenatal US may not detect ectopic kidney, which may be mistaken for a solitary kidney, or severe hydronephrosis (HN), which may be misdiagnosed as MCDK [ 8 ]. Additionally, one-third of patients with CSFK may have extrarenal malformations [ 2 - 3 , 7 , 9 - 11 ]. Therefore, even if a child is diagnosed with CSFK on prenatal US, performing repeat US in the neonatal period to examine for kidney, urinary tract, and other organ malformations is important.

One-third of patients with CSFK have additional congenital anomalies of the kidney and urinary tract (CAKUT) at the solitary functioning kidney [ 1 , 2 ]. Therefore, additional anomalies in the contralateral kidney of MCDK or solitary kidney of renal agenesis should be excluded.

Congenital solitary functioning kidney (CSFK) is characterized by an anatomical or functional absence of one kidney from birth. It includes unilateral renal agenesis (URA), aplasia, and multicystic dysplastic kidney (MCDK). Renal agenesis is characterized by the absence of one kidney, detected via ultrasonography (US) performed at 18–22 gestational weeks, and confirmed postnatally. Aplasia refers to the presence of a rudimentary kidney, observed during the same gestational period, and has a relative function below 5%. MCDK manifests as multiple noncommunicating cysts of various sizes within a lobulated kidney contour, pelvis, and parenchyma. The prevalence of CSFK is approximately 1 in 1,500 newborns [ 1 - 3 ]. Two systematic reviews analyzing large numbers of patients revealed that the prevalence of URA and MCDK is 1 in 2,000 and 1 in 4,300 newborns, respectively [ 2 , 3 ]. Between 6% and 60% of the patients with CSFK have decreased kidney function by the age of 15 [ 4 - 7 ]. However, the possibility of impaired kidney function in CSFK remains debated because of the limited number of studies. Furthermore, CSFK frequently has additional malformations of the kidney, urinary tract, and extrarenal organs. However, as to which, when, and how to test for CSFK remain unclear. This review aimed to describe the publications and recent guidelines, with a focus on optimal evaluation methods for CSFK.

An optimized clinical approach is important for the management of patients with CSFK. Unilateral CSFK carries the potential for hypertension, proteinuria, and progression to chronic kidney disease. However, in those without additional CAKUT and with adequate compensatory growth, routine blood testing is not recommended. Routine DMSA and VCUG are not necessary in all patients with CSFK. In addition, many patients with CSFK are accompanied by extrarenal malformations, among which the Müllerian anomalies can cause infertility, which should always be kept in mind.