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Case Report: Aortic Dissection and Cystic Medial Degeneration in a 24-Year-Old Without Marfan Syndrome

Department of Cardiology, Olive View-UCLA Medical Center, Sylmar, UCLA School of Medicine

Adel El-Bialy, MD

Department of Cardiology, Olive View-UCLA Medical Center, Sylmar, UCLA School of Medicine

The effective management of aortic dissection relies heavily on a high index of suspicion followed by timely definitive diagnosis. Young adults without a history of blunt trauma who are not at risk for atherosclerotic disease may lower this suspicion. We present a 24-year-old patient with complaints of chest pain who presented in multiple urgent care clinics and emergency departments. With a normal chest radiograph, he was repeatedly discharged home on analgesics until a loud murmur was heard. An echocardiogram revealed a dilated aortic root with an intimal flap consistent with a type II dissection. After surgical aortic repair with a Bentall procedure, he was discharged with complete relief of symptoms. Histologic reports revealed cystic medial degeneration. Physical examinations did not demonstrate the phenotypic manifestations of Marfan syndrome. This case illustrates the importance of cardiac auscultation when assessing an individual with chest pain, even with a low likelihood for alteration in arterial structure, and the maintenance of a high index of clinical suspicion despite a normal chest radiograph. We consider this case to be of interest because of its rarity in a 24-year-old.

Key Words: aortic dissection • cardiac auscultation • Marfan syndrome

Journal of Cardiovascular Pharmacology and Therapeutics, Vol. 9, No. 4, 299-302 (2004)
DOI: 10.1177/107424840400900411


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