| Posterior urethral valve | |
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| Classification and external resources | |
Vesiculæ seminales and ampullæ of ductus deferentes, seen from the front. Posterior urethral valves are at the dorsal aspect (back) of the prostatic urethra. |
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| DiseasesDB | 34137 |
| eMedicine | ped/2357 radio/572 |
Posterior urethral valve (PUV) disorder is an obstructive developmental anomaly in the urethra and genitourinary system of male newborns.[1] A posterior urethral valve is an obstructing membrane in the posterior male urethra as a result of abnormal in utero development. It is the most common cause of bladder outlet obstruction in male newborns. The disorder varies in degree, with mild cases followed conservatively. More severe cases can have renal failure and even respiratory failure from lung underdevelopment as result of low amniotic fluid volumes, requiring intensive care and close monitoring.[2]
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Posterior urethral obstruction was first classified by H. H. Young in 1919. The verumontanum, or mountain ridge, is a distinctive landmark in the prostatic urethra, important in the systemic division of posterior valve disorders:
Researchers have suggested that obstructions in the posterior urethra are more appropriately termed congenital obstructions of the posterior urethral membrane (COPUMs). The congenital urothelial remnants of type III posterior urethral valves have been eponymously referred to as Cobb's collar or Moorman's ring.[4]
Abdominal ultrasound is of some benefit, but not diagnostic. Features that suggest posterior urethral valves are bilateral hydronephrosis, a thickened bladder wall with thickened smooth muscle trabeculations, and bladder diverticula.
Voiding cystourethrogram (VCUG) is more specific for the diagnosis. Normal plicae circularis are variable in appearance and often not seen on normal VCUGs. PUV on voiding cystourethrogram is characterized by an abrupt tapering of urethral caliber near the verumontanum, with the specific level depending on the developmental variant. Vesicoureteral reflux is also seen in over 50% of cases.
Diagnosis can also be made by cystoscopy, where a small camera is inserted into the urethra for direct visualization of the posteriorly positioned valve. A limitation of this technique is that posterior valve tissue is translucent and can be pushed against the wall of the ureter by inflowing irrigation fluid, making it difficult to visualize.
Centers in Europe and Japan have also had excellent results with cystosonography, although it has not been approved for use in the United States yet.[5]
Treatment is by endoscopic valve ablation. Fetal surgery is a high risk procedure reserved for cases with severe oligohydramnios, to try to limit the associated lung underdevelopment, or pulmonary hypoplasia, that is seen at birth in these patients. The risks of fetal surgery are significant and include limb entrapment, abdominal injury, and fetal or maternal death. Specific procedures for in utero intervention include infusions of amniotic fluid, serial bladder aspiration, and creating a connection between the amniotic sac and the fetal bladder, or vesicoamniotic shunt.[5]
There are three specific endoscopic treatments of posterior urethral valves:
The standard treatment is primary (transurethral) ablation of the valves.[6] Urinary diversion is used in selected cases,[6] and its benefit is disputed.[7][8]
Following surgery, the follow-up in patients with posterior urethral valve syndrome is long term, and often requires a multidisicplinary effort between general pediatricians, pulmonologists, neonatologists, radiologists and the family of the patient. Care must be taken to promote proper bladder compliance and renal function, as well as to monitor and treat the significant lung underdevelopment that can accompany the disorder.
The female homolog to the male verumontanum from which the valves originate is the hymen.
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