CLASSIFICATION OF
FETAL HYDRONEPHROSIS (1)
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Pyelectasis
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Calectasis
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Pyelectasis
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Grade
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Calyceal Dilatation
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Size of Renal Pelvis
(Antero-posterior
diameter)
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I
II
III
IV
V
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Physiological
dilatation
Normal calyces
Slight dilatation
Moderate dilatation
Severe dilatation + Atrophic cortex
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1 cm
1-1.5 cm
>1.5 cm
>1.5 cm
> 1.5 cm
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Grade
1
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Pyelectasis 8 mm
No caliectasis
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Grade
2
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Grade
3
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Pyelectasis
Caliectasis
No cortical atrophy
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Grade
4
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Pyelectasis
Caliectasis
Ureteric dilatation
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Grade
5
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Pyelectasis
Severe caliectasis
Cortical atrophy
Ureteric dilatation
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Hydronephrosis 28 weeks
Dilated renal pelvis
Global cortical loss
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Same case at 34 weeks
Hydronephrosis
Severe global cortical loss
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- Grignon et al (1) developed a grading system for hydronephrosis in fetuses of 20 weeks gestation or
greater in relation to their postnatal findings. Grade I dilatations (AP
renal pelvic diameter up to 1.0 cm) were described as normal and
physiologic because none of the affected patients required surgery after
birth. Grade II (>1.0–1.5 cm) and grade III (>1.5 cm with
slight dilatation of calices) dilatation was termed intermediate hydronephrosis; 50% required postnatal surgical
intervention. All patients with grade IV dilatation (>1.5-cm pelvis,
moderate dilatation of calices, no cortical atrophy) or grade V hydronephrosis (>1.5-cm pelvis, severe caliceal dilatation, atrophic renal cortex) required
surgery. Their work suggests that one should be concerned with pelvic
dilatations greater than 10 mm particularly if there is associated calyceal dilatation and loss of cortex.
- Corteville et al (2) pointed out that one should be
concerned with lesser degrees of dilatation in fetuses younger than 23 weeks
gestation because these dilatations may be proportional to larger
dilatations in the larger kidneys of older fetuses.
- Langer
et al (3) found 89 (4.4%) of 2170 fetuses with significant renal pelvic
dilatation (described as >5 mm if 28 weeks or less and >10 mm if
>28 weeks). Only 13.7% had postnatal obstruction, reflux, or primary megaureter as the cause. 30.5% had pyelectasis without
obstruction and 55.8% had no abnormality after delivery. They concluded
that one should not consider a pelvis abnormally dilated if <10 mm
after 28 weeks gestation, unless there is concurrent bladder or ureteral dilatation.
- Dremsek et al (4) found prenatal determinations for
dilatation less helpful than postnatal measurements and suggested no need
for concern in a neonate with a renal pelvis AP measurement of <10 mm.
- Degani et al (5) found 67% of 420 mothers who bore a
child with 4 mm or > antenatal renal pelvic dilatation also had a fetus
with pelvic dilatation in their next pregnancy. They suggested a genetic
or environmental influence as the cause of the 6.1 times greater than
normal "risk" for mild pelvic dilatation among siblings.
In the neonatal assessment of antenatal pyelectasis versus hydronephrosis, one must be aware that there is a relative hypovolemia in the first day of life. A false-negative
result may occur when "emergency" US examinations are performed for
the neonate on the day of birth. US evaluations for routine pelvic dilatation
should therefore be made at 2 to 3 days of life (6).
A prominent extra-renal pelvis may
give the appearance that there is renal pyelectasis.

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- Grignon
A, Filion A, Filiatrault
D et.al. Urinary tract dilatation in utero:
classification and clinical applications. Radiology 1986;160:645-647.
- J.E. Corteville,
D.L. Gray and J.P. Crane, Congenital hydronephrosis:
correlation of fetal ultrasonographic findings
with infant outcome. Am J Obstet Gynecol 165
(1991), pp. 384–388.
- B. Langer, U. Simeoni, Y. Montoya et al., Antenatal diagnosis of
upper urinary tract dilation by ultrasonography.
Fetal Diagn Ther 11 (1996), pp. 191–198.
- P. Dremsek,
K. Gindl, P. Voitl et
al., Renal pyelectasis in fetuses and neonates—Diagnostic value of
renal pelvic diameter in pre- and postnatal sonographic screening. Am J Roentgenol 168
(1997), pp. 1017–1019.
- S. Degani,
Z. Leibovitz, I. Shapiro et al., Fetal
pyelectasis in consecutive pregnancies: A possible genetic predisposition.
Ultrasound Obstet Gynecol
10 (1997), pp.
19–21.
- H.L. Cohen and J.O. Haller,
Diagnostic sonography of the fetal genitourinary
tract. Urol Radiol 9 (1987), pp. 88–98.