A Rare Complex Case of Congenital Umbilical Arteriovenous Malformation and Review of Literature

Abstract Introduction Congenital umbilical arteriovenous malformations (AVMs) are extremely rare. We present the first case of congenital umbilical AVM with feeding arteries originating not only from abdominal but also from the mammary arteries. Case Report A 34-week gestational age newborn was tran...

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Main Authors: Rebeca Gregorio-Hernández (Author), Ester Sanz-López (Author), Alejandra Aguado-Del Hoyo (Author), Gema Manrique-Martín (Author), Juan Carlos De-Agustín (Author), Manuel Sánchez-Luna (Author)
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Published: Thieme Medical Publishers, Inc., 2016-06-01T00:00:00Z.
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100 1 0 |a Rebeca Gregorio-Hernández  |e author 
700 1 0 |a Ester Sanz-López  |e author 
700 1 0 |a Alejandra Aguado-Del Hoyo  |e author 
700 1 0 |a Gema Manrique-Martín  |e author 
700 1 0 |a Juan Carlos De-Agustín  |e author 
700 1 0 |a Manuel Sánchez-Luna  |e author 
245 0 0 |a A Rare Complex Case of Congenital Umbilical Arteriovenous Malformation and Review of Literature 
260 |b Thieme Medical Publishers, Inc.,   |c 2016-06-01T00:00:00Z. 
500 |a 2157-6998 
500 |a 2157-7005 
500 |a 10.1055/s-0036-1584239 
520 |a Abstract Introduction Congenital umbilical arteriovenous malformations (AVMs) are extremely rare. We present the first case of congenital umbilical AVM with feeding arteries originating not only from abdominal but also from the mammary arteries. Case Report A 34-week gestational age newborn was transferred to our hospital with a supraumbilical murmur. Abdominal Doppler ultrasound (US) showed a large vascular AVM, with multiple feeding arteries and several venous drainage structures to the umbilical vein and also a persistent ductus venosus. She developed signs of heart failure on the 12th day of life. Computed tomography angiogram revealed an umbilical congenital AVM with feeding arteries originating from the external iliac, hypogastric, epigastric, and mammary arteries and a dilated umbilical vein draining the cluster. Also, a patent ductus venosus was observed. At 14 days of life, laparotomy was performed but due to the complexity of the feeding arteries of the AVM, complete exeresis was not performed, but only ligation of these arteries was made, to reduce the surgical risk. Conclusion To our knowledge, this is the first time that no complete excision was made but only ligation of the arteries. The infant was discharged home on postoperative day 14 being asymptomatic. Follow-up Doppler US showed thrombosed vascular structures. 
546 |a EN 
690 |a arteriovenous malformation 
690 |a congenital 
690 |a high-output cardiac failure 
690 |a newborn 
690 |a Gynecology and obstetrics 
690 |a RG1-991 
655 7 |a article  |2 local 
786 0 |n American Journal of Perinatology Reports, Vol 06, Iss 02, Pp e216-e221 (2016) 
787 0 |n http://www.thieme-connect.de/DOI/DOI?10.1055/s-0036-1584239 
787 0 |n https://doaj.org/toc/2157-6998 
787 0 |n https://doaj.org/toc/2157-7005 
856 4 1 |u https://doaj.org/article/682dbb9bb48c405c834e3e18a3c550b5  |z Connect to this object online.