Acute lower extremity ischaemia after surgical interventricular communication closure in a newborn

2021 ◽  
pp. 1-3
Author(s):  
Nicolas Hugues ◽  
Carine Dommerc ◽  
François Bourlon
Keyword(s):  
Lower Extremity ◽  
Iliac Artery ◽  
Lower Limb ◽  
Rare Case ◽  
Common Iliac Artery ◽  
Artery Dissection ◽  
Acute Ischaemia ◽  
Complete Revascularisation ◽  
The Right

Abstract We report a 5-month-old infant who developed an unexpected acute ischaemia of the right lower limb following a surgical perimembranous interventricular communication closure. This rare case of ischaemia was due to an occlusive right common iliac artery dissection. It was early managed by angioplasty with two ABSORB® bioresorbable stents, resulted in complete revascularisation of the right leg.

A RARE CASE OF MAY- THURNER SYNDROME

2021 ◽  
pp. 17-19
Author(s):  
B. Santhi ◽  
Manigandan Manigandan ◽  
Nishok Nishok
Keyword(s):  
Iliac Artery ◽  
Lower Limb ◽  
Rare Case ◽  
Common Iliac Artery ◽  
Iliac Vein ◽  
Common Iliac Vein ◽  
Middle Aged ◽  
Unique Case ◽  
Left Common Iliac Vein ◽  
Left Lower Limb

May-Thurner syndrome (MTS) is a venous outow obstruction disorder characterized by compression of the left common iliac vein by an overriding right common iliac artery. MTS primarily affects young to middle-aged women, although many patients remain entirely asymptomatic.We report a unique case of a 25 -year-old male who presented with MTS-related multiple varicosities in left lower limb.

scholarly journals Asymptomatic bilateral common iliac artery dissections in previously undiagnosed vascular Ehlers-Danlos syndrome

2019 ◽  
Vol 12 (11) ◽  
pp. e231537
Author(s):  
Matthew Lavoie ◽  
Jason Reese
Keyword(s):  
Iliac Artery ◽  
Common Iliac Artery ◽  
Clinical History ◽  
Artery Dissection ◽  
Intravenous Contrast ◽  
Ehlers Danlos Syndrome ◽  
Left Common Iliac Artery ◽  
Ct Angiogram ◽  
The Right ◽  
Danlos Syndrome

We report a case of a 35-year-old woman found to have vascular Ehlers-Danlos syndrome (vEDS) after family history of sudden death due to aortic dissection in her otherwise healthy brother prompted further imaging workup and consideration of an underlying heritable genetic condition. CT angiogram of the aorta with intravenous contrast revealed an abdominal aortic artery dissection below the level of the renal arteries extending from the bifurcation into the left common iliac artery with an additional focal dissection of the right common iliac artery. To the author’s knowledge, this is the first report of asymptomatic bilateral common iliac artery dissections as a part of the initial presentation of a patient with underlying vEDS. Additionally, this case highlights the importance of familial diagnostic screening in inherited vasculopathies. Clinical history, genetic testing and management are discussed.

Spontaneous Common Iliac Artery Dissection After Exercise

2003 ◽  
Vol 10 (1) ◽  
pp. 163-166 ◽  
Author(s):  
Lip Gen Teh ◽  
Kishore Sieunarine ◽  
Greg van Schie ◽  
Thodur Vasudevan
Keyword(s):  
Iliac Artery ◽  
Common Iliac Artery ◽  
Artery Dissection

Post-operative internal hernia through an orifice underneath the right common iliac artery after Dargent’s operation

Hernia ◽  
2013 ◽  
Vol 18 (6) ◽  
pp. 907-909 ◽  
Author(s):  
M. Ardelt ◽  
Y. Dittmar ◽  
H. Scheuerlein ◽  
E. Bärthel ◽  
U. Settmacher
Keyword(s):  
Iliac Artery ◽  
Internal Hernia ◽  
Common Iliac Artery ◽  
The Right ◽  
Dargent’S Operation
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