Anatomic distribution of renal artery stenosis in children: implications for imaging View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2006-10

AUTHORS

Nghia J. Vo, Ben D. Hammelman, Judy M. Racadio, C. Frederic Strife, Neil D. Johnson, John M. Racadio

ABSTRACT

BACKGROUND: Renal artery stenosis (RAS) causes significant hypertension in children. Frequently, pediatric RAS occurs with systemic disorders. In these cases, stenoses are often complex and/or include long segments. We believed that hypertensive children without comorbid conditions had a different lesion distribution and that the difference might have implications for imaging and treatment. OBJECTIVE: To identify locations of RAS lesions in these hypertensive children without comorbid conditions. MATERIALS AND METHODS: Patients who had renal angiography for hypertension from 1993 to 2005 were identified. Patients with systemic disorders, renovascular surgery, or normal angiograms were excluded. The angiograms of the remaining patients were reviewed for number, type, and location of stenoses. RESULTS: Eighty-seven patients underwent renal angiography for hypertension; 30 were excluded for comorbid conditions. Twenty-one of the remaining 57 patients had abnormal angiograms; 24 stenoses were identified in those patients. All were focal and distributed as follows: 6 (25%) main renal artery, 12 (50%) 2nd order branch, 3 (12.5%) 3rd order branch, and 3 (12.5%) accessory renal artery. CONCLUSION: Hypertensive children without comorbid conditions who have RAS usually have single, focal branch artery stenoses. This distribution supports angiography in these patients because of its superior sensitivity in detecting branch vessel disease and its therapeutic role in percutaneous transluminal renal angioplasty. More... »

PAGES

1032-1036

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s00247-006-0253-8

DOI

http://dx.doi.org/10.1007/s00247-006-0253-8

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1005652399

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/16819600


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