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Type A Aortic Dissection With Intramural Hematoma: A Challenging Diagnosis
Tayseer Kanaan1, Ahmed S Abdelrahman1, Jihad Jaber1
1Cardiology, Hamad Medical Corporation, Doha, QAT.
Insights
Intramural hematoma (IMH), a type of acute aortic syndrome (AAS), can be challenging to diagnose. This case report details a surgically managed Stanford type A IMH with a successful outcome.
Area of Science:
- Cardiovascular Medicine
- Thoracic Surgery
Background:
- Intramural hematoma (IMH) is a critical component of acute aortic syndromes (AAS), encompassing aortic dissection (AD) and penetrating atherosclerotic ulcers (PAU).
- AAS presents similarly but exhibits diverse clinical, pathological, and survival characteristics.
- Accurate classification of IMH, similar to AD, uses systems like Stanford and DeBakey.
Abstract:
Intramural hematoma (IMH) is considered a part of acute aortic syndromes (AAS), a group of life-threatening aortic diseases with a similar presentation that appears to have different clinical manifestations and pathological and survival characteristics. AAS comprises three major entities, namely, aortic dissection (AD), IMH, and PAU. IMH-like classic AD is classified using Stanford and DeBakey classification systems to indicate the aortic area involved. Early diagnosis and treatment of AAS are crucial for survival; however, diagnosis of IMH may be delayed and challenging due to atypical presentation, investigation findings, and case progression. In this report, we describe a case of delayed and challenging diagnosis of a Stanford type A IMH that was managed surgically with a good outcome.
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