Undiagnosed Left
Renal Artery Aneurysm causing maternal and fetal
death in late pregnancy: A case report.
......................................................................................................................................................................
Manar Abu Karaki
Njoud AL-Taleb
Fatima Ali Al-Quran
Ayyed ashamaseen
Rema khlaif al- omosh
Doctor, Gynecology and Obstetrics Department
King Hussein Medical Center
Amman, Jordan
Correspondence:
Dr Njood AL-Taleb
Gynecology and Obstetrics Department
King Hussein Medical Center
Amman, Jordan
Email: nojoodaltaleb@yahoo.com
ABSTRACT
Introduction: Rupture of a renal
artery aneurysm during pregnancy is a rare
event, and is associated with high mortality
and morbidity not only for the mother but
also for the fetus. Increase in cardiac
output and blood volume, with increased
intra-abdominal pressure from enlarging
uterus, and hormonal factors acting on blood
vessel walls causing a relaxation of vascular
walls are predisposing factors to the increased
risk of rupture during pregnancy.
Case presentation: We report a case
of undiagnosed rupture of renal artery aneurysm
in a pregnant woman during
labour. The diagnosis was made during caesarean
section and confirmed by pelvic CT scan
in spite of massive blood transfusion. Unfortunately
the mother and her baby died due to severe
retroperitoneal hemorrhage.
Conclusion: The possibility of a
ruptured renal artery aneurysm should be
considered in pregnant women with evidence
of retroperitoneal hemorrhage.
Key words: aneurysm,
renal artery, pregnancy
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A 35 year old female patient,
Gravida 9 para 8, in her 38th week of pregnancy,
with no significant medical history, presented
to our obstetric unit at Al-karak Military hospital
as labour pain. On examination her blood pressure
was 140/90 mmHg and pulse rate 80 beats per min.
An ultrasound was performed which revealed a viable
fetus in cephalic presentation with normal growth
matching the gestational age. Doppler studies
were within normal values and amniotic fluid was
reported as normal. The cervix was 3 cm dilated.
Three hours after admission in the labour ward
the patient started to have sudden onset of severe
left flank pain associated with nausea. Repeated
vitals were taken; they demonstrated an increase
in heart rate up to 120 beats/min and systolic
blood pressure at 90 mm Hg. Her laboratory values
revealed hemoglobin of 4.7 g/dL and hematocrit
of 15.5%. The patient was aggressively resuscitated
with isotonic fluids and 3 units of packed red
blood cells. She responded appropriately to transfusion.
When stable, she underwent a computed tomography
scan of the abdomen and pelvis which demonstrated
a moderately sized retroperitoneal hematoma surrounding
the left kidney. The patient was taken to the
operating room with suspicion of ruptured uterus;
the patient looked pale with evidence of blood
loss. Re-assessment of the fetus showed absence
of fetal heart motion.
The patient continued to show drop of blood pressure,
90/50, thready pulse of 100 and marked tenderness
to palpation of her left flank.
The patient underwent urgent laparatomy. A classical
caesarean section was performed under another
blood . Four units of whole blood were transfused
rapidly but deterioration continued. Blood pressure
was un-recordable; the pulse volume was very weak.
Still birth fetus was extracted in cephalic presentation
with no signs of obvious structural abnormalities.
There was no active bleeding in the abdominal
cavity but the uterus was pushed to the right
side by a large retroperitoneal hematoma. Hematoma
was opened; left renal artery was seen to be dilated
and ruptured. Trial of clamping of the artery
was performed; at that time the patient arrested
despite having received 21 units of blood.
Renal artery aneurysm (RAA) is
a rare condition, with an incidence ranging between
0.01% and 0.09%, and accounts for 1% of all aneurysms.
In the past this condition was discovered accidentally
or only diagnosed after autopsy(1).
Nowadays with the introduction of angiography
imaging techniques in practice, more frequent
cases have been diagnosed but the incidence is
still low(2).Risk factors for rupture include
incomplete calcification, size >2 cm, progressive
enlargement and pregnancy(3). Rupture of RAA in
a kidney during pregnancy is a rare and well described
catastrophic event, with a high mortality rate
for both mother and fetus(4).
RAA are divided into true and false. True aneurysms
are caused by congenital weakness; atherosclerosis
and trauma. False aneurysms are posttraumatic,
with rupture of the artery and occlusion of the
defect by blood clot.
Reviews of rupture of RAA during pregnancy were
made by Burt in 1956 and by Pedowitz in 1957.
Factors that appear to increase the incidence
of rupture during the third trimester of pregnancy
are: an increase in cardiac output and blood volume,
an increase of intra-abdominal pressure with enlarging
uterus and hormonal factors acting on blood vessel
walls causing a relaxation of vascular walls.
Diagnosis of rupture of RAA during pregnancy is
very difficult as there is no pathognomonic pain
or presentation. When rupture occurs during pregnancy
the clinical presentation is easy to be confused
with those more common conditions like placental
abruption or ruptured uterus as in our case. Most
of the cases were discovered incidentally or after
autopsy. When rupture of RAA occurs during pregnancy
it carries a high fatality or poor feto-maternal
outcomes. When RAA is diagnosed during pregnancy
the treatment modalities, are conservative if
non calcified and small < 2 cm or aneurismal
resection and vascular reconstruction. End to
end anastomosis or nephrectomy is done when the
patient has extensive renal injury or is haemodynamically
unstable. It is usually done as a life saving
procedure.
The clinical presentation of our case was easily
confused with those more common conditions, as
she was thought to have either a placental abruption
or ruptured uterus.
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Dayton et al(4), reported that in a case of ruptured
RAA during pregnancy, the retroperitoneal anatomy
may be severely distorted by massive haematoma.
It may be nearly impossible to determine the exact
anatomy of renal vessels and the presence or absence
of the contra-lateral kidney at the time of surgery.
Spontaneous rupture of RAA is more likely to occur
during pregnancy and when it does, it is associated
with high mortality for both the mother and fetus.
Increased blood flow and intra-abdominal pressure,
and vascular changes secondary to increased steroid
production are postulated as contributory to the
increased risk of rupture of RAA during pregnancy(5).
The possibility of a ruptured
RAA should be considered in pregnant women with
evidence of retroperitoneal hemorrhage.
1) English WP, Pearce JD, Craven
TE, Wilson DB, Edwards MS, Ayerdi J, et al. Surgical
management of renal artery aneurysms. J Vasc Surg
2004;40:53e60.
2) A. Gyedu et al. Surgical Repair of a Giant
Renal Artery Aneurysm: A Case Report. Eur J Vasc
Endovasc Surg (2008) 36, 31e33.
3) Soliman K B, ShawkyY. Ruptured renal artery
aneurysm during pregnancy, a clinical dilemma.
BMC Urology 2006, 6:22.
4) Dayton B, Helgerson RB, Sollinger HW, Acher
CW: Ruptured renal artery aneurysm in a pregnant
uninephric patient: successful ex vivo repair
and autotransplantation. Surgery 1990, 107(6):708-711.
5) Love WK, Robinette MA, Vernon CP: Renal artery
aneurysm ruptures in pregnancy. J Urol 1981, 126(6):809-811.
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