A rare cause and an even rarer treatment of hypertension in a 5‐year‐old boy: Mid‐aortic syndrome

Author:

İriz Erkan1,Tak Sercan1,Yiğiter Eda Nur1,Leventoğlu Emre2ORCID,Demirtaş Hüseyin1,Akkuzu Emine3,Uysal Yazıcı Mutlu3,Fidan Kibriya2,Dalgıç Aydın4

Affiliation:

1. Faculty of Medicine, Department of Cardiovascular Surgery Gazi University Ankara Turkey

2. Faculty of Medicine, Department of Pediatric Nephrology Gazi University Ankara Turkey

3. Faculty of Medicine, Department of Pediatric Intensive Care Gazi University Ankara Turkey

4. Faculty of Medicine, Department of General Surgery Gazi University Ankara Turkey

Abstract

AbstractRenal artery stenosis is one of the common vascular diseases that cause hypertension in children. However, renal artery aneurysms and abdominal aortic aneurysms, which may be components of mid‐aortic syndrome, are rarely associated with renal artery stenosis. Despite its rarity, early diagnosis and treatment are critical to prevent fatal complications. Currently, non‐surgical invasive techniques are considered the first choice for treatment, but in some cases, surgery is inevitable. Here, we present a 5‐year‐old boy with a mid‐aortic syndrome. The patient presented with a history of severe headache and epistaxis 5–6 times a day and was diagnosed with hypertension. A 9 × 9 mm saccular aneurysm on the anterior surface of the abdominal aorta at the level of the left renal artery ostium, and a 12 mm aneurysm in the left renal artery after a stenotic segment at the hilum level was detected in the doppler USG and contrast‐enhanced imaging techniques. The patient was operated on electively. We used a PTFE patch to repair the abdominal aorta and, saphenous vein which was taken from his father to repair the renal artery. The patient recovered well and was discharged on the 18th day.image

Publisher

Wiley

Subject

Nephrology,General Medicine

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