VURD syndrome in an infant presenting with potentially fatal staphylococcal urinary tract infection and septicaemia.

To cite: Ferreira C, Rodrigues M, Reis A, et al. BMJ Case Rep Published online: [please include Day Month Year] doi:10.1136/ bcr-2016-218168 DESCRIPTION A newborn (NB) boy was delivered at 39 weeks of gestation with 4160 g weight and an APGAR score of 8/9. The pregnancy was uneventful, with normal first and second trimester ultrasound. The third trimester ultrasound revealed an isolated right kidney hydronephrosis, a normal sized bladder without thickening of wall as well a normal amniotic fluid volume. Kidney and bladder ultrasound (KBU) scan performed 48 hours after birth showed persistence of right kidney hydronephrosis as well dilation of right ureter. The left kidney and ureter were normal and alteration in bladder volume, bladder wall thickness and posterior urethra were observed. Trimethoprim prophylaxis was started, and the NB was discharged home in good condition. At 1 month age he was revaluated and remained asymptomatic, with an appropriate weight gain. The parents reported normal micturition with good urinary stream, without straining or dribbling. No changes were found on physical examination and the bladder was not palpable. In the second month of life the infant was admitted to the emergency department with fever and urinalysis, collected by urinary stream revealed pyuria. A diagnosis of urinary tract infection (UTI) was suspected and treatment with cefuroxime was initiated. A Staphylococcus haemolyticus sensitive only to vancomycin was isolated in urine and blood cultures, and treatment with vancomycin was initiated. A KBU scan performed revealed persistence of isolated right-sided kidney and ureteral dilation. Fever persisted intermittently during 2 weeks. A voiding cystourethrogram (VC) was performed which showed a right-sided grade V vesicoureteral reflux, a dilation and elongation of the posterior urethra and a linear radiolucent band in distal posterior urethra (figure 1), which confirmed the diagnosis of posterior urethral valves (PUV). Urethrocystoscopy confirmed the presence of PUV and the valves were resected. The infant was discharged home in good condition and no more febrile UTIs were observed. PUVs occur in 1 in 5000 to 1 in 8000 live births and nowadays the diagnosis is frequently suspected in utero with prenatal ultrasound scan showing oligohydramnios, bilateral hydronephrosis, distended bladder and a thickened bladder wall. Frequently PUV newborns may present with unilateral vesicoureteral reflux. VURD (posterior urethral Valve, Unilateral vesicoureteral reflux, Renal Dysplasia) syndrome was identified by Hovver and Duckett in 1982 with the unique relationship between valves, reflux and dysplasia. They noted preserved contralateral renal function into a non-refluxing kidney and proposed that the mechanism of this protection lies in the fact that the refluxing collecting system acts as a pressure pop-off. However, the protective effects of VURD in the long-term has not been as helpful as originally expected. Cuckow et al concluded that renal function deteriorated in patients with VURD syndrome in their cohort of patients on long-term follow-up. About half of the patients with VURD syndrome had renal scarring in the contralateral kidney in the series reported by Narasimhan et al. Independently of presentation the diagnosis of PUV is confirmed by the typical findings of VC. Most common organism in UTI is Escherichia coli, however, unusual organisms including Staphylococcus are encountered in neonates and infants. Primary neonatal methicillinresistant Staphylococcus aureus pyonephrosis has been reported even in a urinary system with unilateral refluxing dilated upper tracts. Figure 1 Voiding cystourethrogram (VC). After filling cystourethrogram a right-sided grade V vesicoureteral reflux was observed (panel A) and VC showed dilation and elongation of the posterior urethra and a linear radiolucent band in distal posterior urethra consistent with the diagnosis of posterior urethral valves (panel B).