Intimomedial mucoid degeneration resulting in a dissecting infrarenal abdominal aortic aneurysm in a young Middle Eastern male: a case report

Author:

Hariri Omar1,Al Laham Omar1,Haffar Lina12,Ghannam Mohammad13,Mohammad Ammar13

Affiliation:

1. Faculty of Medicine, Damascus University, Damascus, (The) Syrian Arab Republic

2. Department of Pathology, Al Assad University Hospital, Damascus University, Damascus, (The) Syrian Arab Republic

3. Department of Vascular and Endovascular Surgery, Al Assad University Hospital, Damascus University, Damascus, (The) Syrian Arab Republic

Abstract

Introduction and importance: Intimomedial mucoid degeneration is a rare vascular disorder first depicted in 1977. It involves mucin deposition in arterial layers. This will cause elastic tissue degeneration and aneurysm formation. This pathology predominantly affects the aorta. However, it could involve other smaller vessels. Surgical treatment could become complicated by a bleeding diathesis. Therefore, a precise surgical technique is necessary to avoid the ensuing complications. Case presentation: We present the case of a previously healthy 27-year-old Middle Eastern male who presented to our surgical clinic following the incidental discovery of an infrarenal abdominal aortic aneurysm following a blunt trauma to the left flank incurred during a fall. Preoperative radiology unveiled a dissecting an infrarenal aortic aneurysm with a concurrent dissection flap at the left renal artery level. Furthermore, an additional dissection flap was observed at the abdominal aortic bifurcation devoid of thrombosis. Clinical discussion: We planned to perform a bilateral aortoiliac bypass. However, due to the fragility of the artery wall, bleeding diathesis, and the tearing that occurred due to the anastomotic suture, the irreparable tear in the anastomosis complicated the situation, we decided to ligate the aorta and perform an axillary-bi-femoral bypass. Conclusion: Intimomedial mucoid degeneration presenting as a dissecting infrarenal abdominal aortic aneurysm is an exceptionally rare pathology. This underscores the crucial need for extensive epidemiological research to document and raise awareness about these cases. Our literature review confirms that our case is the first documented instance in our country, and this emphasizes the significance of our findings.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Reference18 articles.

1. Abdominal aneurysm in South African Negroes due to intimomedial mucoid degeneration;Decker;Br J Surg,1977

2. A young man with intimomedial mucoid degeneration of the brachial artery;Raber;J Vasc Surg,2011

3. Mucoid vasculopathy of unknown etiology;Sandhyamani;Angiology,1991

4. Endovascular treatment of intimomedial mucoid degeneration;Katz;J Vasc Interv Radiol,2008

5. Mucoid degeneration of the brachial artery: case report and a review of literature;Wali;J R Coll Surg Edinb,1999

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