Nephrol Dial Transplant (2000) 15: 415-418
© 2000 European Renal Association-European Dialysis and Transplant Association
Case Reports
Unilateral acute renal cortical necrosis (ACN) following skipping with a rope
David Tovbin1,
Sophie Lantsberg2,
Leonid Feldman1,
Irina Rachinsky2,
Liliana Lupu3 and
Yancu Hertzanu3
1 Division of Nephrology,
2 Nuclear Medicine and
3 Diagnostic Radiology, Soroka Medical Center, Beer-Sheva, Israel
Correspondence and offprint requests to:
David Tovbin MD, Division of Nephrology, Soroka Medical Center, Beer Sheva 84101, Israel.
Keywords: cortical necrosis; rim sign; exercise; vasoconstriction; renal failure
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Introduction
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Unilateral renal cortical necrosis is a rare disorder. The following
is a case report of unilateral renal cortical necrosis in an
18-year-old normally healthy woman following prolonged jumping
over a rope. Extensive work up did not demonstrate any pathology
in the large renal arteries or veins and there was no evidence
of any systemic disease predisposing to thrombosis or disseminated
intravascular coagulation. Though there have been previous reports
of exercise-related unilateral renal infarction associated with
renal artery dissection [
1] or thrombosis [
2], to the best of
our knowledge this is the first report of unilateral cortical
necrosis following physical exercise.
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Case
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An 18-year-old female was admitted to Soroka Medical Center
due to acute right flank and lower quadrant abdominal pain in
the previous few hours. Patient described the onset of acute
pain 30 min after skipping with a rope, with two subsequent
episodes of vomiting. There was no history of any previous illness
and patient denied any medication including oral contraceptives.
On physical examination patient appeared ill and suffering.
Temperature was 37.8°C PR, blood pressure was 125/67 mm
Hg, heart rate was 87 beats/min and there was tenderness over
right flank and in the right lower abdominal quadrant with normal
peristalsis. Complete blood count showed leucocytosis of 16.2
x10
9/l
with 90% neutrophyles, thrombocytosis of 749
x10
9/l, haematocrit
of 42.6% and haemoglobin of 14.2 g/dl. PT and PTT were 12 and
35 s respectively. Urinalysis revealed 10 RBC/HPF. Fractional
excretion of sodium was 2.3%. Initial serum biochemistry results
were urea 5.16 mmol/l, creatinine 124 µmol/l, creatinine
phosphokinase of 150 IU/l, aspartate aminotransferase 105 IU/l,
alanine aminotransferase 111 IU/l, lactate dehydrogenase 2260
IU/l. After an emergent ultrasound without evidence of renal
abscess or hydronephrosis, explorative laparotomy and appendectomy
were performed due to the clinical presentation of peritoneal
irritation and suspicion of acute appendicitis, with evidence
for mesenteric lymphadenitis. Pain persisted and repeated renal
ultrasound demonstrated hyperechogenic right kidney (not shown).
Colour Doppler showed reduced perfusion and decreased demonstration
of intra-renal blood vessels in the right kidney in the presence
of patent renal artery and vein, and normal left kidney. A Tc-99m-DTPA
(diethylenetriamine pentaacetic acid) renal scan (Figure 1

)
demonstrated almost complete absence of perfusion and poor function
of the right kidney, with normal perfusion, function and excretion
in the left kidney. Renal artery or venous thrombosis were strongly
suspected and a subsequent renal angiography demonstrated patent
main and segmental renal arteries with capsular arterial supply
of the upper pole but no appearance of the interlobular or arcuate
arteries. The renal parenchyma appeared as a mottled nephrogramme
and there was no early filling of the renal veins. Angiography
(Figure 2

) and venography (not shown) which were completely
normal did not show renal artery or venous thrombosis and since
the diagnosis still remained unclear, an enhanced helical computerized
tomography scan was performed. A region of low attenuation of
the right kidney (representing the non-enhancing necrotic cortex),
a normal signal from the medulla, a thin rim of enhanced subcapsular
region (a rim sign) and no excretion of the contrast medium
were found (Figure 3

). These results were consistent with acute
unilateral renal cortical necrosis. Tc-99m-DMSA (dimercaptosuccinic
acid) scan was performed to confirm the diagnosis of cortical
necrosis and to assess the extent of the damage. This scan demonstrated
a small section of viable cortex of the upper pole surrounded
by a wide-rimmed photopenic area indicative of cortical loss
which correlated well with the angiographic findings. Protein
S was 74.1% (normal 70140), anti thrombin III 99.7% (normal
82122), protein C 117.7% (normal 70130), APC resistance
V 2.28 (normal 25), C3 96 mg% (normal 80200),
C4 24 mg% (normal 1647), anti-cardiolipin antibodies
levels IgM of 1.1 U/ml (normal 07) and IgG of 2.9 U/ml
(normal 010). Rheumatoid factor and antinuclear antibody
were negative. Cardiac echocardiography and ventilationperfusion
lung scan were normal. After 36 h serum creatinine level reached
132.6 mmol/l but at 72 h decreased to 97.2 mmol/l and after
5 weeks to 88.4 mmol/l. Since Mag-3 (mercaptoacetylglycine)
is actively excreted through the proximal renal tubules and
thus superior to DTPA for imaging of kidneys with impaired function,
a Mag-3 renal scan was performed 10 days later as a follow-up
procedure. This scan demonstrated a small shrunken right kidney
with very delayed perfusion and 17% of differential function.
An enhanced CT scan 5 weeks later demonstrated a small shrunken
right kidney with a preserved nephrographic cortical effect
and a clear cortico-medullary differentiation with a slight
increase in size of the contra lateral kidney. On ultrasound
the right kidney was 7.9 cm and the left kidney was 11.9 cm.
In summary, this patient had a unique clinical course of unilateral
cortical necrosis following physical exercise.

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Fig. 1. DTPA renal study. Posterior view: each image represents the sum of 3 min of dynamic sequential images. The study showed an absence of perfusion and function of the right kidney. Perfusion, function and excretion in the left kidney are normal.
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Fig. 2. Selective right renal angiography shows a disorganized intrarenal vasculature, with no filling of the interlobular and arcuate arteries and the presence of capsular vessels of upper renal pole.
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Fig. 3. Early spiral enhanced CT after bolus injection of contrast media shows right kidney with enhancement of the medulla, non- enhancement of the renal cortex, a thin rim of enhanced subcapsular tissue (`rim sign') and lack of excretion of the contrast material into the collecting system. The left kidney is normal.
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Discussion
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In this paper we describe an 18-year-old woman with acute unilateral
cortical necrosis following physical exercise (rope skipping).
Acute appendicitis was suggested by the clinical picture of
peritoneal irritation but was excluded by explorative laparotomy,
similar to a previous report of a polar infarct of kidney transplant
[
3]. The differential diagnosis of acute unilateral renal-related
pain, reduction in renal function and fever, includes infectious
and obstructive processes, but ultrasound did not demonstrate
hydronephrosis or abscess. Thus, the differential diagnosis
narrowed down to acute unilateral renal vascular events associated
with renal necrosis, which was suggested in our patient by the
clinical picture of flank pain and increase in serum levels
of LDH, AST and alkaline phosphatase. Acute renal vein thrombosis
which has been described in an adult male with vomiting induced
volume depletion [
5], and associated with medullary necrosis
in a renal allograft [
6], was excluded by renal venography.
Renal infarction is usually induced by interference of arterial
flow in large and medium renal arteries due to direct trauma
[
4] or embolic disease [
7]. Unilateral renal infarction post
exercise has been described related to arterial thrombosis [
2],
and renal artery dissection [
1], which were excluded in our
patient by renal arteriography. Renal artery torsion has been
previously described in kidney transplants [
8
10], one
of which was associated also with lack of abdominal support
due to prune belly syndrome [
10]. Renal artery spasms have been
reported following renal angioplasty [
11]. However, in our patient
the eventuality of transient arterial disturbances seemed remote,
since there was no direct stimulation of renal artery and the
only putative aetiology for renal artery torsion could be a
change in position induced by the act of skipping. The imaging
studies were pathognomic for unilateral ACN with unaffected
contra-lateral kidney [
12
19]. Acute cortical necrosis
is a rare cause of acute renal failure, related to constriction
of small intracortical blood vessels with disturbed blood flow
to interlobular and afferent arterioles but usually sparing
the arcuate arteries. The subsapsular rim of cortex, a thicker
layer under the corticomedullary junction, and some parts of
the cortex may be spared due to collateral flow through multiple
capsular anastomosa via the lumbal, intercostal, inferior adrenal
and middle capsular arteries [
12]. The appearance of enhanced
CT has been shown to be pathognomic and diagnostic for ACN.
The four features on CT that typify ACN include: enhancement
of the medulla, non-enhancement of the renal cortex, a thin
rim of enhanced subcapsular tissue (`rim sign') explained by
presence of collateral blood supply, and lack of excretion of
the contrast material into the collecting system. This disorder
is usually associated with states of endothelial damage such
as complications of pregnancy, sepsis, disseminated intra-vascular
coagulation or haemolytic-uraemic syndrome [
20]. Unilateral
cortical necrosis has been previously described in renal transplantation
[
21], and in the contra-lateral kidney of kidneys with ureteral
obstruction or malignancy [
22], contrary to our patient in whom
the contra-lateral kidney was intact. In addition to renal infarction,
there have been reports of exercise-induced acute renal failure
related to severe vasoconstriction and acute tubular necrosis
[
23]. However, to the best of our knowledge this is the first
account of unilateral cortical necrosis following exercise without
damage to main renal vessels. The aetiology for unilateral cortical
necrosis in this patient is not clear and may include a rare
combination of predisposing factors, each of them in itself
not sufficient to induce this extremely rare pathologic process.
Physical exercise has been demonstrated to be associated with
renal vasoconstriction, reduction in renal cortical flow and
increase in renal cortical resistance, probably due to immediate
activation of

-adrenergic receptors by the renal nerves and
subsequently by humural mediators [
24], that theoretically might
be augmented in the presence of oestrogen in a female patient
[
25]. Exercise-induced thrombocytosis and later reactive thrombocytosis
may be associated potentially with release of serotonin which
might have contributed to renal vasoconstriction [
26]. However,
there is still no clue to a main predisposing factor which might
have induced unilateral endothelial damage and cortical necrosis.
As pain was described to be extremely acute at the onset, renal
artery torsion due to position changes could be a remote hypothetical
possibility. In conclusion, we have presented here a unique
case of unilateral renal cortical necrosis following the act
of skipping with a rope.
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Received for publication: 16. 8.99
Accepted in revised form: 17.11.99

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