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Michael P. D'Alessandro, M.D.
Peer Review Status: Internally Peer Reviewed
Clinical History:
This newborn full term female was noted to have ascites on her
prenatal ultrasound. During her vaginal delivery, the abdomen could
not be delivered due to its large size. Delivery was finally
accomplished after removing 200 cc of ascites from the baby by
placing a needle through the abdominal wall and uterus of the mother.
Clinical Physical Exam:
Upon delivery the baby was noted to have a midline defect including a
split anterior half of the sternum, an omphalocele and a
thoracoabdominal ectopic cordis.
Clinical Labs:
Non-contributory
Clinical Differential Diagnosis:
Pentalogy of Cantrell
Imaging Findings:
A chest and abdominal film from the first day of life demonstrated
the ectopia cordis and a paucity of bowel gas in the abdomen.
Abdominal US from the second day of life (not provided) demonstrated
massive ascites, and no hepatic lesions were seen. An echocardiogram
noted the presence of double outlet right ventricle.
Imaging Differential Diagnosis:
Ectopia cordis
Operative Findings:
On the second day of life the patient was taken to the operating room
for closure of the midline defect. The midline defect extended from
just below the umbilicus to halfway up the heart and was a few
centimeters wide. The omphalocele sac was excised revealing the apex
of the heart and the liver. The pericardium was intact. The diaphragm
was intact. The omphalocele was closed by approximating the abdominal
fascia. The heart was covered with skin.
Pathological Findings:
None
Final Diagnosis:
Pentalogy of Cantrell
Follow-up and Prognosis:
The patient had an uncomplicated post-operative course. A chest CT
exam was performed at 2 weeks of life and demonstrated a very
hypoplastic appearing anterior chest wall and a stenosis of the left
mainstem bronchus as the cause of the patient's left lung
hyperinflation. This was confirmed by endoscopy 3 days later which
showed this compression to be due to a pulsating vessel.
Similar Cases:
None
References:
None
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