Key result
Aortic stenting immediately normalizes severe hypertension in Takayasu-related abdominal coarctation.
Why the study?
Abdominal aortic coarctation is a rare cause of severe hypertension in adolescents and is often associated with Takayasu arteritis.
Case Report (n=1)
Endovascular stenting is an effective treatment for severe hypertension caused by abdominal aortic coarctation secondary to Takayasu arteritis in adolescents.
Endovascular stenting may relieve hypertension in adolescent Takayasu-related abdominal aortic coarctation; hypothesis-generating pending prospective data.
BACKGROUND: Abdominal aortic coarctation (AAC) is a rare cause of severe hypertension in adolescents and is often associated with Takayasu arteritis. CASE SUMMARY: We present a case of a 15-year-old boy with a 4-month history of progressive dyspnea and easy fatiguability. He was found to have severe systemic hypertension, radiofemoral delay, and a significantly higher upper limb blood pressure (BP) compared with lower limb BP. Computed tomography aortography demonstrated severe AAC. He underwent successful endovascular intervention with stenting of the abdominal aorta. Hypertension and symptoms resolved immediately postintervention. DISCUSSION: AAC may occur as a congenital anomaly or secondary to inflammatory conditions such as Takayasu arteritis, particularly in young individuals with severe hypertension. This case underscores the value of physical examination and imaging in the evaluation of a young patient with hypertension. TAKE-HOME MESSAGE: Severe hypertension with radiofemoral delay and an upper-to-lower limb BP gradient >20 mm Hg prompted evaluation for AAC.
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Oladimeji et al. (2026) conducted a case report in Abdominal aortic coarctation secondary to Takayasu arteritis (n=1). Endovascular stenting was evaluated. Endovascular stenting of the abdominal aorta in a 15-year-old boy with abdominal aortic coarctation secondary to Takayasu arteritis resulted in immediate reduction of blood pressure from 200/120 mm Hg to 102/68 mm Hg.
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