FRINK Linked Data Fragments server

Matches in SemOpenAlex for { <https://semopenalex.org/work/W2115379576> ?p ?o ?g. }

• W2115379576 endingPage "1063" @default.
• W2115379576 startingPage "1063" @default.
• W2115379576 abstract "Editor:We read with interest the article by Chen et al (1Chen W Chu J Yang JY et al.Endovascular stent placement for the treatment of nutcracker phenomenon in three pediatric patients.J Vasc Interv Radiol. 2005; 16: 1529-1533Abstract Full Text Full Text PDF PubMed Scopus (29) Google Scholar) concerning endovascular stent placement for the treatment of nutcracker phenomenon in three pediatric patients. Nutcracker syndrome is attributable to idiopathic decrease in the angle between the aorta and the superior mesenteric artery with consequent compression of the left renal vein, and surgical procedures such as Gore-Tex graft vein interposition, nephropexy, and kidney autotransplantation are available to correct the compression of the left renal vein (2Russo D Minutolo R Iaccarino V et al.Gross hematuria of uncommon origin: the nutcracker syndrome.Am J Kidney Dis. 1998; 32: E3Abstract Full Text Full Text PDF PubMed Google Scholar). However, endovascular stent treatment has recently been suggested as a safer and more efficient technique than surgical procedures and may represent a valuable approach to the treatment of adult nutcracker syndrome (3Hartung O Grisoli D Boufi M et al.Endovascular stenting in the treatment of pelvic vein congestion caused by nutcracker syndrome: lessons learned from the first five cases.J Vasc Surg. 2005; 42: 275-280Abstract Full Text Full Text PDF PubMed Scopus (108) Google Scholar). Nevertheless, the invasive treatment of childhood nutcracker syndrome is still under debate.Our previous report (4Shin JI Park JM Lee SM et al.Factors affecting spontaneous resolution of hematuria in childhood nutcracker syndrome.Pediatr Nephrol. 2005; 20: 609-613Crossref PubMed Scopus (91) Google Scholar) demonstrated that aortomesenteric compression could resolve spontaneously within a relatively short time (mean, 1.4 y; range, 0.5–3.5 y) as a result of physical development during childhood. Although a major factor affecting the decrease of the peak flow velocity in the aortomesenteric portion of the left renal vein was the increase in body mass index, the increase in diameters of the left renal vein by growth might also influence the renal hemodynamics.These findings suggest that the first therapy for hematuria of childhood nutcracker syndrome should be observation. However, in our study, some patients showed persistent hematuria despite the decrease of the peak velocity in the aortomesenteric portion of the left renal vein, indicating that these patients might require therapy.Therefore, we believe that endovascular stent placement should be considered when this syndrome leads to persistent clinical symptoms after a sufficiently long period of observation, and should be guided by the clinical, radiologic, and renal hemodynamic findings. We suggest that the period of observation should be at least 2 to 3 years, because 15 of the 20 patients with nutcracker syndrome (75%) showed complete resolution of hematuria within 3 years of follow-up. Further studies and long-term follow-up are necessary before endovascular stent placement is accepted for the treatment of childhood nutcracker syndrome. Editor: We read with interest the article by Chen et al (1Chen W Chu J Yang JY et al.Endovascular stent placement for the treatment of nutcracker phenomenon in three pediatric patients.J Vasc Interv Radiol. 2005; 16: 1529-1533Abstract Full Text Full Text PDF PubMed Scopus (29) Google Scholar) concerning endovascular stent placement for the treatment of nutcracker phenomenon in three pediatric patients. Nutcracker syndrome is attributable to idiopathic decrease in the angle between the aorta and the superior mesenteric artery with consequent compression of the left renal vein, and surgical procedures such as Gore-Tex graft vein interposition, nephropexy, and kidney autotransplantation are available to correct the compression of the left renal vein (2Russo D Minutolo R Iaccarino V et al.Gross hematuria of uncommon origin: the nutcracker syndrome.Am J Kidney Dis. 1998; 32: E3Abstract Full Text Full Text PDF PubMed Google Scholar). However, endovascular stent treatment has recently been suggested as a safer and more efficient technique than surgical procedures and may represent a valuable approach to the treatment of adult nutcracker syndrome (3Hartung O Grisoli D Boufi M et al.Endovascular stenting in the treatment of pelvic vein congestion caused by nutcracker syndrome: lessons learned from the first five cases.J Vasc Surg. 2005; 42: 275-280Abstract Full Text Full Text PDF PubMed Scopus (108) Google Scholar). Nevertheless, the invasive treatment of childhood nutcracker syndrome is still under debate. Our previous report (4Shin JI Park JM Lee SM et al.Factors affecting spontaneous resolution of hematuria in childhood nutcracker syndrome.Pediatr Nephrol. 2005; 20: 609-613Crossref PubMed Scopus (91) Google Scholar) demonstrated that aortomesenteric compression could resolve spontaneously within a relatively short time (mean, 1.4 y; range, 0.5–3.5 y) as a result of physical development during childhood. Although a major factor affecting the decrease of the peak flow velocity in the aortomesenteric portion of the left renal vein was the increase in body mass index, the increase in diameters of the left renal vein by growth might also influence the renal hemodynamics. These findings suggest that the first therapy for hematuria of childhood nutcracker syndrome should be observation. However, in our study, some patients showed persistent hematuria despite the decrease of the peak velocity in the aortomesenteric portion of the left renal vein, indicating that these patients might require therapy. Therefore, we believe that endovascular stent placement should be considered when this syndrome leads to persistent clinical symptoms after a sufficiently long period of observation, and should be guided by the clinical, radiologic, and renal hemodynamic findings. We suggest that the period of observation should be at least 2 to 3 years, because 15 of the 20 patients with nutcracker syndrome (75%) showed complete resolution of hematuria within 3 years of follow-up. Further studies and long-term follow-up are necessary before endovascular stent placement is accepted for the treatment of childhood nutcracker syndrome." @default.
• W2115379576 created "2016-06-24" @default.
• W2115379576 creator A5029688026 @default.
• W2115379576 creator A5038504015 @default.
• W2115379576 creator A5046452850 @default.
• W2115379576 date "2006-06-01" @default.
• W2115379576 modified "2023-10-12" @default.
• W2115379576 title "Re: Endovascular Stent Placement for the Treatment of Nutcracker Phenomenon in Three Pediatric Patients" @default.
• W2115379576 cites W1994246932 @default.
• W2115379576 cites W2015390855 @default.
• W2115379576 cites W2093906897 @default.
• W2115379576 cites W2145885067 @default.
• W2115379576 doi "https://doi.org/10.1097/01.rvi.0000222649.68037.82" @default.
• W2115379576 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/16778244" @default.
• W2115379576 hasPublicationYear "2006" @default.
• W2115379576 type Work @default.
• W2115379576 sameAs 2115379576 @default.
• W2115379576 citedByCount "13" @default.
• W2115379576 countsByYear W21153795762012 @default.
• W2115379576 countsByYear W21153795762013 @default.
• W2115379576 countsByYear W21153795762015 @default.
• W2115379576 countsByYear W21153795762017 @default.
• W2115379576 countsByYear W21153795762018 @default.
• W2115379576 countsByYear W21153795762019 @default.
• W2115379576 countsByYear W21153795762021 @default.
• W2115379576 countsByYear W21153795762022 @default.
• W2115379576 crossrefType "journal-article" @default.
• W2115379576 hasAuthorship W2115379576A5029688026 @default.
• W2115379576 hasAuthorship W2115379576A5038504015 @default.
• W2115379576 hasAuthorship W2115379576A5046452850 @default.
• W2115379576 hasBestOaLocation W21153795761 @default.
• W2115379576 hasConcept C126322002 @default.
• W2115379576 hasConcept C126838900 @default.
• W2115379576 hasConcept C141071460 @default.
• W2115379576 hasConcept C2778583881 @default.
• W2115379576 hasConcept C2779774813 @default.
• W2115379576 hasConcept C2780091579 @default.
• W2115379576 hasConcept C2781046184 @default.
• W2115379576 hasConcept C2781278258 @default.
• W2115379576 hasConcept C2910216633 @default.
• W2115379576 hasConcept C2911204043 @default.
• W2115379576 hasConcept C71924100 @default.
• W2115379576 hasConceptScore W2115379576C126322002 @default.
• W2115379576 hasConceptScore W2115379576C126838900 @default.
• W2115379576 hasConceptScore W2115379576C141071460 @default.
• W2115379576 hasConceptScore W2115379576C2778583881 @default.
• W2115379576 hasConceptScore W2115379576C2779774813 @default.
• W2115379576 hasConceptScore W2115379576C2780091579 @default.
• W2115379576 hasConceptScore W2115379576C2781046184 @default.
• W2115379576 hasConceptScore W2115379576C2781278258 @default.
• W2115379576 hasConceptScore W2115379576C2910216633 @default.
• W2115379576 hasConceptScore W2115379576C2911204043 @default.
• W2115379576 hasConceptScore W2115379576C71924100 @default.
• W2115379576 hasIssue "6" @default.
• W2115379576 hasLocation W21153795761 @default.
• W2115379576 hasLocation W21153795762 @default.
• W2115379576 hasOpenAccess W2115379576 @default.
• W2115379576 hasPrimaryLocation W21153795761 @default.
• W2115379576 hasRelatedWork W1521914646 @default.
• W2115379576 hasRelatedWork W1821744383 @default.
• W2115379576 hasRelatedWork W1997613030 @default.
• W2115379576 hasRelatedWork W2007001560 @default.
• W2115379576 hasRelatedWork W2091988232 @default.
• W2115379576 hasRelatedWork W2158003420 @default.
• W2115379576 hasRelatedWork W2601369883 @default.
• W2115379576 hasRelatedWork W2788696935 @default.
• W2115379576 hasRelatedWork W2979696249 @default.
• W2115379576 hasRelatedWork W3029641154 @default.
• W2115379576 hasVolume "17" @default.
• W2115379576 isParatext "false" @default.
• W2115379576 isRetracted "false" @default.
• W2115379576 magId "2115379576" @default.
• W2115379576 workType "article" @default.