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Description
A 52-year-old Caucasian woman with a history of hypertension since age 30 was referred to cardiology department due to aortic stenosis. She had exertional dyspnoea, without thoracic pain or syncope. There was no blood pressure gradient between upper and lower extremities. Transthoracic echocardiography revealed bicuspid aortic valve, severe valvular aortic stenosis and dilation of ascending aorta (figure 1). There was also a tapering of the descending aorta, with turbulent flow and a systolic peak gradient of 19 mm Hg (figure 2). To assess the thoracic aorta, the patient underwent CT angiography, which revealed elongation of the distal aortic arch, a focal kinking at the aortic isthmus, and absence of significant stenosis and enlarged collateral arteries, consistent with aortic pseudocoarctation (figure 3).
Aortic pseudocoarctation is a very rare congenital anomaly of the aortic arch and can coexist with other congenital heart diseases, such as bicuspid aortic valve.1 It mimics true coarctation, but can be differentiated from it by recognising a high, elongated arch, a kinking that lacks luminal narrowing and an absence of enlarged collateral arteries.2 The identification of aortic pseudocoarctation can be an incidental finding or associated with hypertension and symptoms related to compression of adjacent structures.1 Its management is not well established, but surgical treatment has been proposed in symptomatic patients or when associated with aortic aneurysms.3 The case was discussed in a multidisciplinary team, and it was decided that the pseudocoarctation did not require intervention and should be regularly monitored for changes in the aorta. Thus, the patient was submitted to aortic valve replacement with mechanical prosthetic valve and ascending aorta replacement surgery. The cardiac surgery was uneventful.
Learning points
Aortic pseudocoarctation is a very rare congenital anomaly that mimics coarctation, but lacks significant luminal narrowing and enlarged collateral arteries.
Although less severe than true coarctation, it should not be regarded as a benign condition. Surgical treatment has been proposed in symptomatic patients or when associated with aortic aneurysms, and regular follow-up in asymptomatic patients without associated anomalies.
This case highlights the importance of echocardiographic suprasternal view to identify aortic coarctation or pseudocoarctation as a cause of secondary hypertension.
Footnotes
Contributors All authors made substantial contributions to the conception or design of the work, or the acquisition, analysis or interpretation of data; helped in drafting the work or revising it critically for important intellectual content; and approved the final version submitted to this journal. FC drafted the article. SSC, AF and JIM revised the article critically for important intellectual content. All authors approved the final version submitted to BMJ Clinical Cases and agreed to be accountable for the article and to ensure that all questions regarding the accuracy or integrity of the article are investigated and resolved.
Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.
Competing interests None declared.
Patient consent Obtained.
Provenance and peer review Not commissioned; externally peer reviewed.