Acute renal failure as a presentation of an aortocaval fistula associated with abdominal aortic aneurism.

نویسندگان

  • M Arruche Herrero
  • V Ruiz García
  • A I Castillo Escudero
  • C Gómez Miranda
  • N Rodríguez Espinosa
  • C Villavicencio Luján
  • A Martínez Vea
چکیده

1. Rousaud F, Palacín M, Nunes V. Cistinuria. Nefrología 2003;23 Suppl 1:52-9. 2. Milliner DS, Murphy ME. Urolithiasis in pediatric patients. Mayo Clin Proc 1993; 68:241-8. 3. Brasseur-Daudruy M, Garel C, Brossard V, Broux F, Heckettsweiler B, Eurin D. Hyperechogenic colon: a prenatal sign of cystinuria? Prenat Diagn 2006;26:1254-5. 4. Merieau E, Cloarec S, Benoist JF, Haddad G, Benoit S, Nivet H. An antenatal hyperechogenic colon: question. Pediatr Nephrol 2009;24:277-9.

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Aortocaval Fistula: A Rare Cause of Venous Hypertension and Acute Renal Failure

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Aortocaval fistula (ACF) is an unusual complication of ruptured abdominal aortic aneurysm (AAA), involving less than 3-6% of all ruptured cases. The clinical presentation is often obscure, depending on the coexistence of retroperitoneal rupture and hemodynamic instability. Prompt preoperative diagnosis is essential in order to plan the operative approach and improve patient's outcome. We report...

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Surgical repair of ruptured abdominal aortic aneurysm with non-bleeding aortocaval fistula.

We present a case of an aortocaval fistula (ACF) without bleeding because a clot was covering the fistula. A 60-year-old man was diagnosed as having a ruptured abdominal aortic aneurysm (AAA) and an aortocaval fistula, by enhanced computed tomography (CT). After the aneurysm had been opened, the fistula was detected, but there was no bleeding because it was covered with clot. After graft repair...

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Multiple aortocaval fistulas associated with a ruptured abdominal aneurysm in a patient with Ehlers-Danlos syndrome.

Aortocaval fistula (ACF) is a rare complication of spontaneous abdominal aortic aneurysm (AAA) rupture, with an incidence of 2-4%. A unique case of ruptured AAA complicated by multiple aortovenous fistulas involving the inferior vena cava and left internal iliac vein is presented, and is the first published report of a patient with Ehlers-Danlos syndrome undergoing surgical treatment for an ACF.

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عنوان ژورنال:
  • Nefrologia : publicacion oficial de la Sociedad Espanola Nefrologia

دوره 31 1  شماره 

صفحات  -

تاریخ انتشار 2011