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15

Pathophysiology of Renal Obstruction

Glenn M. Cannon and Richard S. Lee

Causes of Renal Obstruction

Renal obstruction can be caused by intrinsic or extrinsic factors that affect the ureters, bladder, or urethra. Most of the literature concerning the pathophysiology of renal obstruction has focu­ sed on unilateral ureteral obstruction (UUO) or bilateral ureteral obstruction (BUO). Table 15.1 lists possible causes of renal obstruction.

Effects on Prenatal Development

Prenatal Hydronephrosis

Ultrasound has remained the main diagnostic tool in evaluation of prenatal hydronephrosis since its introduction in 1980.1 Historically, the degree of anteroposterior renal pelvic diameter has been used as an indicator to predict need for surgery.A renal pelvic diameter of <12 mm with­ out caliectasis poses a minimal risk of eventually requiring surgery, while severe dilatation of >50 mm may inevitably require surgery.1 Diuretic renal scanning aids the evaluation of infants between these two extremes and has been dem­ onstrated to be reliable over the age of 6 weeks to 2 months.2 Serial ultrasound examination is fre­ quently utilized and a trend of progressive hydro­ nephrosis on two consecutive examinations serves as an early diagnostic sign of obstruc­ tion.3 Society of Fetal Urology (SFU) Grade of 3–4 of postnatal hydronephrosis and a relative

renal function of <40% are both independent risk factors for the eventual need for surgery.

Lee et al. performed a meta­analysis includ­ ing 1,308 patients with prenatal hydronephrosis and postnatal follow­up that concluded that children with any degree of prenatal hydroneph­ rosis are at greater risk of postnatal pathology compared with the normal population.4 They found that children with moderate hydroneph­ rosis (defined as AP diameter 7–10 mm for sec­ ond trimester, 9–15 mm for third trimester) and severe hydronephrosis (AP diameter > 1m for second trimester, >15 mm for third trimester) were at significant risk for postnatal pathology, and postnatal diagnostic studies should be con­ sidered. The authors also concluded that even children with mild prenatal hydronephrosis may carry a greater risk as compared to the normal population for postnatal pathology. The optimal postnatal management of patients with mild prenatal hydronephrosis is controversial and further prospective studies are needed.

Spectrum of Renal Abnormalities

Congenital ureteropelvic junction obstruction (UPJO) can cause a spectrum of renal abnor­ malities.5,6 In its mildest form, UPJO represents the radiological demonstration of reversible hydronephrosis without permanent renal dam­ age. Its most severe form represents a hypertro­ phic and fibrotic UPJ with renal parenchymal changes such as glomerulosclerosis, chronic tubulointerstitial injury, and dysplasia that may

C.R. Chapple and W.D. Steers (eds.), Practical Urology: Essential Principles and Practice,

197

DOI: 10.1007/978-1-84882-034-0_15, © Springer-Verlag London Limited 2011

 

198

Practical Urology: EssEntial PrinciPlEs and PracticE

Table 15.1. Possible causes of renal obstruction

 

Urethral stricture

 

 

 

 

 

 

Ureter

 

Urethral carcinoma

 

 

 

 

 

 

Intrinsic

 

Urethral atresia

 

 

 

 

 

 

Ureteropelvic junction obstruction

Extrinsic

 

 

 

 

 

 

 

Ureterovesical junction obstruction

 

Prostate carcinoma

 

 

 

 

 

 

Ureteral valve

 

Penile carcinoma

 

 

 

 

 

 

Ureteritis cystica

 

 

 

 

 

tuberculosis

 

 

 

 

 

schistosomiasis

necessitate nephrectomy.7 Renal biopsies per­

Ureteral carcinoma

formed in patients after pyeloplasty demon­

strate relatively well­maintained parenchyma in

Papillary necrosis

which the only overt changes are mainly

calculus

glomerular.7

 

 

 

Endometriosis

 

 

 

 

 

Blood clot

 

 

 

 

 

Fungal bezoar

Signaling Pathways and Tissue

 

Extrinsic

Interactions

 

 

crossing lower pole vessel at ureteropelvic junction

Recent finding from gene expression studies

retroperitoneal fibrosis

and embryological mutants have resulted in a

better understanding of ureteral development

retroperitoneal tumor

and its effect on the developing renal paren­

abdominal aortic aneurysm

chyma. Glial­derived neurotropic factor (Gdnf)

is released from the metanephric blastema and

cervical cancer

induces ureteral bud growth from the Wolffian

Prostate cancer

duct.8 Airik et al. have demonstrated that the

retrocaval ureter

transcription

factor gene

Tbx18 is

initially

expressed between the Wolffian duct and meta­

 

tubo-ovarian abscess

nephric mesenchyme in mouse embryos and is

diverticulitis

later

found exclusively at

the distal

ureteric

stalk.9 This implies that the ureteric mesen­

 

gravid uterus

chyme is differentiated shortly after ureteral

Bladder

budding, which occurs before the differentia­

tion of ureteric epithelium. Several investiga­

 

Intrinsic

tors have identified that the signaling molecule

Bladder carcinoma

Bmp4 also plays a key role in the specification

and differentiation of the ureteric bud.10­12

calculi

Both urothelial and smooth muscle develop­

neurogenic bladder

ment are significantly impaired after inactiva­

tion of the Bmp4 gene. Deletion of the signaling

Extrinsic

molecule Bmp4 or the angiotensin type II

Pelvic lipomatosis

receptor can result in ectopic Gdnf signaling

Urethra

that

results

in multiple

ureteric

buds.13­15

Multiple other genes have been identified as

 

Intrinsic

playing a role in ureteral development and

Posterior urethral valve

mutations in any of them may result in urinary

tract obstruction.8