- Research Article
- 10.4103/aca.aca_79_25
Porcelain Aorta in Young: A Rare Encounter.
- Jan 01, 2026
- Annals of cardiac anaesthesia
- Ankita Singh + 3 more +3
To the Editor, The term porcelain aorta, defined as an extensive calcification of the aorta, increases the complexity of cardiac surgery. Although usually seen in the elderly population, we report a rare and unprecedented finding of a porcelain aorta incidentally discovered in a patient in his twenties. A 29-year-old male patient with prior Bentall surgery in 2014 for ascending aorta aneurysm and aortic regurgitation (AR) presented with suprasternal swelling [Figure 1] and fever, revealing calcification of bilateral common carotid artery and arch of the aorta in chest X-ray (CXR) posterior-anterior (PA) view [Figure 2]. Contrast-enhanced computed tomography (CECT) thorax revealed dense peripheral wall calcification of bilateral common carotid artery, arch of the aorta, and descending thoracic aorta; also, aneurysmal dilation of the aortic arch and right subclavian artery; and narrowing of descending thoracic aorta. The patient was taken for emergency exploration because the swelling was increasing with an associated drop in hemoglobin. Intraoperatively, the patient was found to have a mediastinal abscess draining into subcutaneous space and drained under femoral bypass. The patient was shifted to the intensive care unit on vasopressor support and was extubated on postoperative day one, but later, he succumbed to sepsis.Figure 1: Suprasternal swellingFigure 2: CXR PA view showing bilateral carotid artery, aortic arch calcification and intercoastal drain in situ (for hydropneumothorax)Porcelain aorta is challenging because it precludes aortic cannulation and cross-clamping due to the risk of injury and release of thromboembolic material, causing stroke. Peripheral arterial cannulation, intraluminal balloon occlusion of the aorta, hypothermic circulatory arrest to avoid cross-clamping, and slow aortic clamping with flushing through the open aorta can minimize this risk.[1] Vascular calcification has been reported in younger patients with chronic kidney disease (due to altered mineral metabolism), systemic lupus erythematosus (SLE), and Takayasu arteritis due to systemic inflammation and immune mechanisms.[2] Our patient had a normal renal function test and no history of claudication, joint pain, or skin rashes. Tests for SLE were not performed. He fulfilled one major criterion (fever) and three minor criteria (previous history of AR, descending thoracic aorta narrowing, and high ESR, 40 mm/hr in our case) of the Sharma criteria for diagnosis of Takayasu arteritis, but using fever as a major criterion is dubious in the background of mediastinal abscess.[3] Boudagh et al.[3] had reported a similar case of Takayasu arteritis in a young patient with severe AR and atypical presentation. Unfortunately, the focus was on determining the reason for suprasternal swelling, and other findings on CECT were not thoroughly investigated. CT angiography, which depicts luminal changes and is a reliable tool in the diagnosis of Takayasu arteritis, was not performed, and rheumatology consultation was also not sought. Genetic predilection and chronic inflammation post-cardiac surgery might have led to accelerated vascular fibrosis and calcification in this patient, or he might have some underlying vasculitis that remained undiagnosed and Takayasu arteritis should also be kept in mind as a cause of AR and aortic aneurysm in young patients. Declaration of patient consent The authors certify that they have obtained all appropriate patient consent forms. In the form, the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed. Financial support and sponsorship Nil. Conflicts of interest There are no conflicts of interest.
Read more