scholarly journals A Case of Blue Toe Syndrome and Myonephropathic Metabolic Syndrome with Abdominal Aortic Aneurysm.

1994 ◽  
Vol 23 (5) ◽  
pp. 340-344
Author(s):  
Hiroshi Sato ◽  
Masao Okamura ◽  
Masayoshi Okada ◽  
Hitoshi Matsuda
2005 ◽  
Vol 4 (4) ◽  
pp. 391-393 ◽  
Author(s):  
Paulo Eduardo Ocke Reis

The authors report the case of a man with blue toe syndrome, who developed bilateral foot ischemia and underwent successful repair of an abdominal aortic aneurysm and associated renal artery stenosis. Blue toe syndrome is characterized by tissue ischemia secondary to embolization of cholesterol crystals or atherothrombotic debris. Microembolization most often occurs in elderly men who undergo an invasive vascular procedure or have an aneurysm.


2014 ◽  
Vol 59 (4) ◽  
pp. 938-943 ◽  
Author(s):  
Michael R. Hall ◽  
Clinton D. Protack ◽  
Roland Assi ◽  
Willis T. Williams ◽  
Daniel J. Wong ◽  
...  

2014 ◽  
Vol 142 (3-4) ◽  
pp. 229-232
Author(s):  
Petar Popov ◽  
Slobodan Tanaskovic ◽  
Vuk Sotirovic ◽  
Srdjan Babic ◽  
Dragoslav Nenezic ◽  
...  

Introduction. Severe extremity ischemia and the presence of the ?blue-toe? syndrome are rarely the first complications of the present abdominal aortic aneurysm. We report two interesting cases of this rare entity. Outline of Cases. A 61-year-old man presented with the rest pain of his toes accompanied with digital ischemia of both feet. Physical examination confirmed regular arterial pulses at lower extremities accompanied with palpable pulsate mass in the abdomen. Vascular ultrasound and multidetector tomography (MDCT) of blood vessels revealed small abdominal aortic aneurysm (37 mm in diameter), filled with the irregular, ulcerated, heterogeneous thrombotic masses. Aneurysm sac resection was performed with an aorto-bi-iliac bypass reconstruction. A week later, it was mandatory to amputate the fifth toe on the left foot because of the advanced gangrenous process. The second case was a 77-year-old woman with 7-day history of severe feet pain. Abdominal examination revealed pulsatile mass paraumbilical to the left. Performed abdominal ultrasonography and MDCT angiography confirmed coexistence of the infrarenal aortic aneurysm, 40.5 mm in diameter, covered by significant mobile mural thrombus and ulcerations. Surgical reconstruction was mandatory and patient underwent aneurysm sac resection and aortobifemoral reconstruction. Conclusion. Embolic phenomenon and peripheral embolic occlusion from the mural thrombus within the abdominal aortic aneurysm are relatively rare events, but associated with tissue loss. Thorough diagnostic examinations and prompt management are required regardless of the aneurysm size once these signs occurred.


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