Middle Aortic Syndrome
- 1 September 1986
- journal article
- Published by Wolters Kluwer Health in Annals of Surgery
- Vol. 204 (3) , 331-339
- https://doi.org/10.1097/00000658-198609000-00012
Abstract
Middle aortic syndrome typically occurs as severe hypertension in young patients who have weak or absent femoral pulses and an abdominal bruit. It results from a diffuse narrowing of the distal thoracic and abdominal aorta, commonly involving the visceral and renal arteries. The clinical presentation, angiographic assessment, and surgical outcome of 10 patients (mean age: 19.5 years) who underwent one-stage revascularization for middle aortic syndrome were reviewed to determine the effectiveness and durability of one-stage revascularization techniques to relieve these complications. All patients were hypertensive (mean blood pressure: 176 mmHg); six (60%) had severe, poorly controlled hypertension, two of whom had previous failed operations for renovascular hypertension and one who presented with malignant hypertension and acute renal failure. Five patients had disabling myocardial insufficiency, only one of whom had documented coronary artery disease. Four patients had intermittent claudication. Aortography showed variable length high-grade midaortic stenosis, nine had visceral artery involvement, and eight had renal artery involvement. All patients underwent one-stage revascularization by a variety of autogenous and prosthetic techniques. The postoperative recovery was uncomplicated in eight of nine patients and was often associated with dramatic reduction in blood pressure. There was a single death from disruption of the thoracic anastomosis in a patient who had diffuse cystic medial necrosis of the aorta. Arterial biopsy in nine patients indicated evidence for both acquired and congenital origins of the midaortic stenosis. Late follow-up evaluation (mean: 4.1 years) showed normal growth and development, preservation of renal function, and relief of myocardial insufficiency in all patients. Seven patients (77%) are cured of their hypertension, and two (23%) have only mild hypertension. These results indicate that one-stage revascularization of patients with middle aortic syndrome can result in effective and durable relief of these severe life-threatening complications.Keywords
This publication has 14 references indexed in Scilit:
- Takayasu's arteritis and atypical coarctation--the same disease.1983
- Aortorenal Arterial AutograftsArchives of Surgery, 1981
- Coarctation of the Abdominal AortaAnnals of Surgery, 1980
- Coarctation of the Abdominal Aorta: Pathophysiologic and Therapeutic ConsiderationsAnnals of Surgery, 1979
- Takayasu's arteritis and congenital coarctation of the descending thoracic and abdominal aorta: a critical reviewAmerican Journal of Roentgenology, 1976
- Hypoplasia of the Abdominal Aorta Associated With the Rubella SyndromeArchives of Pediatrics & Adolescent Medicine, 1970
- COARCTATION OF THE ABDOMINAL AORTA IN CHILDREN: REPORT OF THREE CASES AND REVIEW OF THE LITERATUREPediatrics, 1969
- Coarctation of the Abdominal AortaCardiology, 1969
- Coarctation Of The Abdominal Aorta With Renal Arterial StenosisAnnals of Surgery, 1967
- Coarctation of the Abdominal AortaJapanese Heart Journal, 1964