Successful surgical repair of critical ascending and descending aortic aneurysms at nine-year intervals in Wiskott-Aldrich syndrome: A case report

Mehmet Akif Önalan

doi:10.5606/tgkdc.dergisi.2023.22506

Mehmet Akif Önalan¹, Hüsnü Fırat Altın¹, Murat Çiçek¹, Okan Yurdakök¹, Ahmet Şaşmazel¹

¹Department of Pediatric Cardiac Surgery, Dr. Siyami Ersek Thoracic Heart and Vascular Surgery Training and Research Hospital, Istanbul, Türkiye

DOI : 10.5606/tgkdc.dergisi.2023.22506

Wiskott-Aldrich syndrome is an uncommon X-linked inherited disorder related to primary immunodeficiency, infections, eczema, and thrombocytopenia. A 21-year-old male patient with this syndrome underwent descending aortic aneurysm repair at the age of 12. The patient had ascending aortic aneurysm with aortic valve regurgitation and surgical aortic root replacement was performed. To the best of our knowledge, this is the first case with Wiskott-Aldrich syndrome operated due to aneurysms development in different segments of the thoracic aorta in both childhood and young adult periods.

Keywords : Aortic aneurysm, aortic valve, thoracic aorta, Wiskott- Aldrich syndrome

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