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ABSTRACT
OBJECTIVE. We sought to assess the clinical and imaging findings in intermittent
hydronephrosis secondary to ureteropelvic junction obstruction, with particular
emphasis on the characteristic ultrasonographic findings.
METHODS. This prospective, longitudinal, observational study included all children
who had intermittent ureteropelvic junction obstruction and presented with abdominal pain over 6 years. Renal ultrasound was used as an initial screening tool
to detect intermittent hydronephrosis. Renal ultrasonography was repeated every
1 to 2 days to record serial changes from the symptomatic to the asymptomatic
stage. Their clinical manifestations and imaging findings were studied.
RESULTS. Eighteen patients (14 boys, 4 girls) were studied. Most had sharp pain that
began acutely and typically lasted for 2 days. Most of the children (16 of 18) had
nausea and vomiting that accompanied the pain. The acute episode generally
resolved spontaneously and was followed by a pain-free interval that ranged from
days to months. Factors that predisposed to an attack included increased water
intake, vigorous exercise, or bladder distention. All patients had clearly demonstrable obstruction of the renal pelvis during an acute attack, a finding that
diminished or resolved during the symptom-free intervals. During convalescence,
all patients had renal pelvic wall thickening on ultrasonography. This finding
appeared on the second or third day after a painful episode subsided, persisted for
6 to 9 days, and then disappeared in the symptom-free stage. Pyeloplasty was
performed in 17 patients, none of whom had recurrent pain on follow-up. Extrinsic obstructions were found in 9 patients.
www.pediatrics.org/cgi/doi/10.1542/
peds.2005-0583
doi:10.1542/peds.2005-0583
Key Words
intermittent hydronephrosis,
ureteropelvic junction obstruction,
prospective studies, renal
ultrasonography, renal pelvic wall
thickening, convalescence, intravenous
pyelogram, diuretic renal scan,
computed tomography, dismembered
pyeloplasty, follow-up
Abbreviations
UPJO ureteropelvic junction
obstruction
IVPintravenous pyelogram
VCUGvoiding cystourethrography,
CT computed tomography
DTPA diethylene triamine
pentaacetic acid
Accepted for publication Jun 20, 2005
Address correspondence to Pei-Yeh Chang,
MD, Department of Pediatric Surgery, Chang
Gung Childrens Hospital, 5-7, Fu-Hsin St,
Kwei-Shan, Taoyuan, Taiwan. E-mail:
pyjchang@cgmh.org.tw
PEDIATRICS (ISSN 0031 4005). Copyright 2006
by the American Academy of Pediatrics
139
METHODS
From July 1998 to May 2004, all children who had
intermittent hydronephrosis and presented with abdominal pain were studied prospectively. Informed consent
was obtained from the parents of the children. The diagnosis of intermittent hydronephrosis required all of
the following criteria: (1) episodes of intermittent abdominal pain were associated with demonstrable UPJO
only during an attack or on provocative testing8; (2)
urinary tract infection was ruled out by finding a negative urine culture and no evidence of pyonephrosis on
ultrasonography; (3) vesicoureteral reflux was ruled out
by voiding cystourethrography (VCUG); (4) a renal
stone in the ureteropelvic junction was excluded by
plain abdominal film, ultrasonography, or computed tomography (CT) when necessary; and (5) the imaging
studies demonstrated obstructive hydronephrosis during
an acute attack but no obstruction during symptom-free
intervals.
Renal ultrasound was used as an initial screening tool
to detect intermittent hydronephrosis. All ultrasound
examinations were performed by 1 pediatric nephrologist using a Toshiba (Tokyo, Japan) SSA-260A scanner
with a 3.5-MHz transducer. The urinary tract was examined in both supine and prone positions. Hydronephrosis
140
TSAI, et al
n (%)
16 (89)
2 (11)
1 (6)
14 (78) (Right: 2, left: 12)
4 (22)
4 (22)
1 (6)
6 (33)
10 (56)
2 (11)
3 (17)
3 (17)
6 (33)
4 (22)
2 (11)
FIGURE 1
CT of ruptured kidney. The patient had intense pain that woke him from sleep in the
morning. CT showed rupture of the right kidney with perinephric uid collection. Bloody
urine was drained via a percutaneous nephrostomy.
6 (33)
3 (17)
4 (22)
7 (39)
n (%)
(N 18)
16 (89)
4 (22)
2 (11)
7 (39)
2 (11)
1 (6)
1 (6)
1 (6)
1 (6)
Grade 2
Grade 3
Grade 4
10
8
2
141
FIGURE 2
Serial ultrasound ndings from the acute episode through to recovery. A, This 8-year-old boy had severe hydronephrosis at the painful stage. The pain lasted for 2 days. B, On the
second day after the pain had subsided, the size of hydronephrosis was gradually decreased. C. On the third day, the hydronephrosis was continuously decreased in degree, and
thickened pelvic wall was examined (arrowheads). D, The measured thickness of the pelvic wall was 3.2 mm in the prone position (arrowheads). E, The thickened pelvic wall persisted
for 6 days and disappeared on the ninth day.
TSAI, et al
143
TSAI, et al
obstruction may have resolved so that the hydronephrosis has disappeared or there remains only mild dilation of
the renal pelvis. Mild hydronephrosis can occur in patients with normal variants, bladder distention, vesicoureteral reflux, and chronic nonobstructive hydronephrosis. In addition, hydronephrosis can be found in
asymptomatic children, with a reported prevalence in
schoolchildren of 0.193% by portable ultrasound
screening.23 Therefore, the question is how to determine
when mild hydronephrosis indicates previous obstruction that has resolved, rather than some other condition.
From our study, we think that renal pelvic wall thickening on ultrasonography during convalescence is an
important clue to recent dilation of the pelvis. According
to Robben et al,24 the normal pelvic wall thickness in
normal children ranges from 0.1 to 0.8 mm. They suggested a threshold of 0.8 mm as a reliable discriminator
for pathologic conditions. All of our patients had much
thicker pelvic walls, ranging from 2.5 to 5.6 mm. A
thickened pelvic wall is reported to occur in various
diseases, including acute pyelitis,9,2426 vesicoureteral reflux,9,2426 rejection of a renal transplant,27 acute tubular
necrosis,28 congenital hydronephrosis after pyeloplasty,28
mobile nephrolithiasis,29 and structural causes of intermittent dilation of the collecting system.24
Three groups have mentioned the relationship between UPJO and pelvic wall thickening. Babcock et al28
first reported it in patients with UPJO after pyeloplasty.
Sorantin et al26 reported 4 cases of UPJO with renal
pelvic wall thickening, but the clinical presentation in
those cases was not described. Robben et al24 recently
evaluated the significance of renal pelvic wall thickening
and found that intermittent dilation of the collecting
system was an important cause. If vesicoureteral reflux
is excluded, then the differential diagnosis of a thickened
renal pelvic wall includes a high-pressure bladder, primary obstructing megaureter, and UPJO. However,
none of these studies determined the incidence of pelvic
wall thickening, the timing of its occurrence, or the
duration of recovery in patients with intermittent hydronephrosis. In all of our patients, pelvic wall thickening appeared on the second or third day after a painful
episode subsided, at the time when the degree of hydronephrosis was gradually beginning to decrease. The
thickened wall then persisted for 6 to 9 days and disappeared during the symptom-free stage, when very slight
pelvic dilation was present.
The pathophysiology of renal pelvic wall thickening
in intermittent hydronephrosis relates to the acute ureteral obstruction that produces hyperperistalsis and high
intrapelvic pressure.30 The thickening of the wall may be
caused by subepithelial edema or an acute inflammatory
response of the collecting systems. Increased stretching
of the pelvis and high intrapelvic pressure further traumatize the wall, inducing additional edema and inflammation. However, during an acute episode, significant
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