<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>41(3)</volume><submitter>Plonsky Toder M</submitter><funding>Technion - Israel Institute of Technology</funding><pubmed_abstract>&lt;h4>Background&lt;/h4>Takayasu arteritis (TAK) is a granulomatous large-vessel vasculitis typically affecting young adult females. Pediatric cases are rare, and infantile onset is exceptional. Management relies on immunosuppression, with surgery reserved for severe complications.&lt;h4>Case report&lt;/h4>We describe a now 5.5-year-old boy diagnosed with TAK at six months of age, presenting with hypertensive encephalopathy and kidney dysfunction. Despite treatment with corticosteroids and anti-TNFα, his kidney function deteriorated, leading to kidney failure and dialysis. At nearly three years of age, he underwent abdominal aorto-aortic bypass and bilateral nephrectomy due to progressive vascular narrowing and refractory hypertension. At age four, he successfully received a deceased-donor kidney tra</pubmed_abstract><journal>Pediatric nephrology (Berlin, Germany)</journal><pagination>873-881</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12852304</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Navigating complex clinical decisions: kidney transplantation following abdominal aorto-aortic bypass in infantile Takayasu arteritis.</pubmed_title><pmcid>PMC12852304</pmcid><pubmed_authors>Plonsky Toder M</pubmed_authors><pubmed_authors>Magen D</pubmed_authors><pubmed_authors>Tibi R</pubmed_authors><pubmed_authors>Steinberg R</pubmed_authors><pubmed_authors>Karram T</pubmed_authors><pubmed_authors>Eisenstein I</pubmed_authors><pubmed_authors>Coleman D</pubmed_authors><pubmed_authors>Pollack S</pubmed_authors><pubmed_authors>Libinson-Zebegret I</pubmed_authors><pubmed_authors>Hoffman A</pubmed_authors><pubmed_authors>Yakubov R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Navigating complex clinical decisions: kidney transplantation following abdominal aorto-aortic bypass in infantile Takayasu arteritis.</name><description>&lt;h4>Background&lt;/h4>Takayasu arteritis (TAK) is a granulomatous large-vessel vasculitis typically affecting young adult females. Pediatric cases are rare, and infantile onset is exceptional. Management relies on immunosuppression, with surgery reserved for severe complications.&lt;h4>Case report&lt;/h4>We describe a now 5.5-year-old boy diagnosed with TAK at six months of age, presenting with hypertensive encephalopathy and kidney dysfunction. Despite treatment with corticosteroids and anti-TNFα, his kidney function deteriorated, leading to kidney failure and dialysis. At nearly three years of age, he underwent abdominal aorto-aortic bypass and bilateral nephrectomy due to progressive vascular narrowing and refractory hypertension. At age four, he successfully received a deceased-donor kidney tra</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Mar</publication><modification>2026-06-16T03:16:01.752Z</modification><creation>2026-06-16T03:09:42.138Z</creation></dates><accession>S-EPMC12852304</accession><cross_references><pubmed>40932502</pubmed><doi>10.1007/s00467-025-06932-w</doi></cross_references></HashMap>