Aged ; Aneurysm, False ; complications ; Aortic Aneurysm, Thoracic ; complications ; Aortic Diseases ; etiology ; Esophageal Fistula ; etiology ; Humans ; Male

Aged ; Aortic Diseases ; complications ; Esophageal Diseases ; etiology ; Humans ; Intestinal Fistula ; complications ; Jejunal Diseases ; complications ; Male ; Tomography, X-Ray Computed ; Ulcer ; etiology ; Vascular Fistula ; complications

Acute Disease ; Adult ; Aortic Diseases ; diagnosis ; etiology ; Arterial Occlusive Diseases ; diagnosis ; etiology ; Heart Neoplasms ; complications ; Humans ; Male ; Myxoma ; complications

We report a case of surgically treated abdominal aortic aneurysm (AAA) in a patient having crossed ectopia with fusion anomaly of the kidney. One artery from the abdominal aorta above the aneurysm supplies the right kidney while three renal arteries (two from the aneurysm itself and one from the left common iliac artery) supply the crossed ectopic kidney. Preoperative imaging to define the arterial and collecting systems along with a detailed planning of the operation is essential to prevent ischemic renal injury as well as ureteral injury during AAA repair.
Aged ; Aortic Aneurysm, Abdominal/*complications/pathology/*surgery ; Choristoma/*complications/pathology ; Human ; *Kidney ; Kidney Diseases/*complications/pathology ; Magnetic Resonance Angiography ; Male

Although cervical epidural abscess is rare, it should be strongly suspected in any patient with unexplainable neck pain and fever, especially when the patient has a predisposing factor for this infectious process. The authors report a case of cervical epidural abscess in a 39-yr-old man with an aorto-duodenal fistula, which complicated the interposition of artificial graft for abdominal aortic aneurysm rupture, which had undertaken 40 months before. Timely detection and intervention rendered him a full neurological recovery. This extremely rare case is presented with a literature review.
Adult ; Aneurysm, Dissecting/complications ; Aneurysm, Dissecting/surgery ; Aortic Aneurysm, Abdominal/complications ; Aortic Aneurysm, Abdominal/surgery ; Aortic Diseases/complications* ; Aortic Rupture/complications ; Aortic Rupture/surgery ; Blood Vessel Prosthesis Implantation ; Cervical Vertebrae* ; Duodenal Diseases/complications* ; Duodenal Ulcer/complications ; Enterococcus ; Epidural Abscess/etiology* ; Epidural Abscess/microbiology ; Epidural Abscess/surgery ; Fistula/complications* ; Gram-Positive Bacterial Infections/complications ; Human ; Male ; Peptic Ulcer Perforation/complications ; Salmonella Infections/complications ; Staphylococcal Infections/complications

Interrupted aortic arch is a rare congenital vascular malformation associated with a high mortality rate in infancy, and is therefore very unusual in adults. We report a case of interrupted aortic arch in a 42-year-old male hypertensive patient who was found to have a disruption of aorta continuity distal to the left subclavian artery with massive collateral circulation into the descending aorta by computed tomography angiography. The patient was discharged after the blood pressure was controlled by antihypertensive therapy. This case suggests the necessity of careful auscultation for young patients with hypertension. Once murmur in the chest and back is heard, computed tomography angiography should be performed at once to avoid missed diagnosis and misdiagnosis.
Adult ; Aorta, Thoracic ; pathology ; Aortic Diseases ; complications ; Humans ; Hypertension ; etiology ; Male

OBJECTIVETo evaluate the effect of reduction aortoplasty for dilatation of the ascending aorta in patients with aortic valve disease.

METHODSBetween February 1998 and May 2004, 23 patients with aortic valve disease and dilatation of the ascending aorta underwent reduction aortoplasty in combination with aortic valve replacement. The diameter of the ascending aorta was measured before and early after surgery and then later between 4 and 78 months [mean (36 +/- 25) months] postoperatively using echocardiography.

RESULTSThe reduction aortoplasty decreased the diameter of the aorta from (4.8 +/- 0.5) cm preoperatively to (3.6 +/- 0.4) cm early after surgery (P < 0.01). During follow-up, the diameter of aorta increased from (3.6 +/- 0.4) cm early after surgery to (3.7 +/- 0.4) cm after a mean follow-up of (36 +/- 25) months (P < 0.05).

CONCLUSIONReduction aortoplasty shows good mid-term results in patients with aortic valve disease and dilatation of the ascending aorta. Long-term results need to be followed up.

Adult ; Aged ; Angioplasty ; methods ; Aorta ; surgery ; Aortic Diseases ; complications ; surgery ; Aortic Valve Insufficiency ; complications ; surgery ; Aortic Valve Stenosis ; complications ; surgery ; Female ; Follow-Up Studies ; Heart Valve Prosthesis Implantation ; Humans ; Male ; Middle Aged ; Treatment Outcome

Abdominal aortoenteric fistula (AAEF) is a rare but life-threatening complication of abdominal aortic aneurysms, and is also an uncommon cause of gastrointestinal hemorrhage. We report a case of primary abdominal aortoduodenal fistula in a 74-year-old male patient, whose main clinical manifestations were abdominal pain, hematochezia, and hematemesis. Colonoscopy, abdominal enhanced computed tomography (CT) and three-dimensional reconstruction angiography confirmed the diagnosis. The patient recovered well after emergent surgical management.
Abdominal Pain ; Aged ; Angiography ; Aortic Aneurysm, Abdominal ; complications ; Aortic Diseases ; Colonoscopy ; Duodenal Diseases ; Gastrointestinal Hemorrhage ; Humans ; Intestinal Fistula ; Male ; Tomography, X-Ray Computed

A 68-year-old woman with known severe aortic stenosis was admitted to the hospital because of hematochezia and dizziness. She had received several blood transfusions over the preceding 3 years and undergone right hemicolectomy 2 years ago for severe lower gastrointestinal bleeding. Postoperative histology revealed angiodysplasia involving the ascending colon. After the hemicolectomy, she continued to have hematochezia and anemia and required additional blood transfusions for anemia. During this admission, platelet count, activated partial-thromboplastin time, von Willebrand factor antigen, and von Willebrand factor ristocetin cofactor were normal. She had a severe deficiency of high-molecular-weight multimers of von Willebrand factor. Colonoscopy showed angiodysplasia in the transverse colon at this time. Successful coagulation of the bleeding angiodysplasia was achieved by argon plasma coagulator. No additional bleeding was observed thereafter. We report a case of Heyde's syndrome with abnormal von Willebrand factor in a patient who presented with intestinal angiodysplasia and aortic stenosis.
Aged ; Anemia/etiology/therapy ; Angiodysplasia/*complications ; Aortic Valve Stenosis/*complications ; Colonic Diseases/*complications ; English Abstract ; Female ; Gastrointestinal Hemorrhage/*etiology ; Humans ; Syndrome ; von Willebrand Disease/*complications/diagnosis

Aortic Diseases ; complications ; etiology ; Esophageal Fistula ; complications ; etiology ; Female ; Hematemesis ; etiology ; Humans ; Middle Aged ; Tuberculosis, Miliary ; complications ; Vascular Fistula ; complications ; etiology