Thorac Cardiovasc Surg 2003; 51(6): 350-352
DOI: 10.1055/s-2003-45430
Original Paper
© Georg Thieme Verlag Stuttgart · New York

Obstructed Coarctation in a Right Aortic Arch in an Adult Female

T.  Kaneda1 , S.  Miyake1 , T.  Kudo2 , T.  Ogawa1 , T.  Inoue1 , T.  Matsumoto1 , M.  Onoe1 , S.  Nakamoto1 , H.  Kitayama1 , T.  Saga1
  • 1Departments of Cardiovascular Surgery and
  • 2Radiology, Kinki University School of Medicine, Ohno-Higashi, Osaka-Sayama City, Osaka, Japan
Further Information

Publication History

Received June 23, 2003

Publication Date:
11 December 2003 (online)

Abstract

Coarctation of a right aortic arch is rare congenital anomaly. We report a rare case of a 24-year-old female with coarctation of the right aortic arch with aberrant left subclavian artery between the right common carotid and right subclavian arteries. The coarctation progressed into complete obstruction as the interruption of the aorta in adulthood. To prevent cerebral complications and progression to heart failure, surgical procedure was selected. Extraanatomical bypass grafting between the ascending and descending aorta was successfully performed using cardiopulmonary bypass. Some patients diagnosed with interruption of the aortic arch in adulthood might be displaying progression of undiagnosed coarctation, as our in case. Three-dimensional computed tomography was useful to detect the obstructive lesion and to determine the surgical approach and methods.

References

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Correspondence

MD, PhD Toshio Kaneda

Department of Cardiovascular Surgery, Kinki University School of Medicine

377-2, Ohno-Higashi

Osaka- Sayama City

Osaka 589-8511

Japan

Phone: +81/723/ 67-86 57

Fax: +81/723/67-86 57

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