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http://dx.doi.org/10.3345/kjp.2016.59.11.S84

Idiopathic midaortic syndrome with malignant hypertension in 3-year-old boy  

Ahn, Kyung Jin (Department of Pediatrics, Seoul National University Children's Hospital)
Yoon, Ja Kyoung (Department of Pediatrics, Seoul National University Children's Hospital)
Kim, Gi Beom (Department of Pediatrics, Seoul National University Children's Hospital)
Kwon, Bo Sang (Department of Pediatrics, Seoul National University Children's Hospital)
Bae, Eun Jung (Department of Pediatrics, Seoul National University Children's Hospital)
Noh, Chung Il (Department of Pediatrics, Seoul National University Children's Hospital)
Publication Information
Clinical and Experimental Pediatrics / v.59, no.sup1, 2016 , pp. 84-87 More about this Journal
Abstract
Midaortic syndrome (MAS) is a rare vascular disease that commonly causes renovascular hypertension. The lumen of the abdominal aorta narrows and the ostia of the branches show stenosis. MAS is associated with diminished pulses in the lower extremities compared with the upper extremities, severe hypertension with higher blood pressure in the upper rather than lower extremities, and an abdominal bruit. The clinical symptoms are variable, and recognition in children with hypertension can aid early diagnosis and optimal treatment. Hypertension with MAS is malignant and often refractory to several antihypertensive drugs. Recently, radiologic modalities have been developed and have led to numerous interventional procedures. We describe the case of a 3-year-old boy presenting with left ventricular hypertrophy whose severely elevated blood pressure led to the diagnosis of idiopathic MAS. This case highlights the importance of measuring blood pressure and conducting a detailed physical examination to diagnose MAS. This is the first reported case of idiopathic MAS diagnosed in childhood in Korea.
Keywords
Aortic coarctation; Renovascular hypertension; Renal artery obstruction;
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