Literature DB >> 1752898

A case of congenital hypoplasia of the right external iliac artery.

R Seghezzi1, G Rossi, F Chierichetti, M Lovotti, M Salvini.   

Abstract

A 18 years male had congenital hypoplasia of the right external iliac artery and thrombosis of its narrowest part. Congenital megacolon, anal atresia and hyposomical nanism were also present. Surgical intervention was indicated because he was developing arterial insufficiency and muscular hypotrophy of the right leg. A bypass was performed with a reversed autogenous vein between the common iliac artery and the common femoral artery.

Entities:  

Mesh:

Year:  1991        PMID: 1752898

Source DB:  PubMed          Journal:  J Cardiovasc Surg (Torino)        ISSN: 0021-9509            Impact factor:   1.888


  3 in total

1.  Congenital Absence of the Right Common Iliac Artery.

Authors:  Donnette A Dabydeen; Anatoli Shabashov; Kitt Shaffer
Journal:  Radiol Case Rep       Date:  2015-11-06

2.  Preservation of internal iliac artery flow during endovascular aortic aneurysm repair in a patient with bilateral absence of common iliac artery.

Authors:  Minh-Anh Pham; Thanh-Phong Le
Journal:  J Vasc Surg Cases Innov Tech       Date:  2021-01-28

3.  Novel, congenital iliac arterial anatomy: Absent common iliac arteries and left internal iliac artery.

Authors:  Christopher S Green; Mohammed A Helmy
Journal:  Radiol Case Rep       Date:  2015-11-06
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.