2018
DOI: 10.1007/s00428-018-2500-4
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Botryoid Wilms tumor: a non-existent “entity” causing diagnostic and staging difficulties

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Cited by 14 publications
(14 citation statements)
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“…The predisposing syndromes associated with BGP were scarcely described. Among 77 patients (8 BWT), Vujanić et al 2 reported only 1 patient with Denys-Drash syndrome. In our cases, 2 children had a WT1 mutation, in relation with the bilateral disease.…”
Section: Discussionmentioning
confidence: 99%
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“…The predisposing syndromes associated with BGP were scarcely described. Among 77 patients (8 BWT), Vujanić et al 2 reported only 1 patient with Denys-Drash syndrome. In our cases, 2 children had a WT1 mutation, in relation with the bilateral disease.…”
Section: Discussionmentioning
confidence: 99%
“…In literature, nephrogenic rests were found in 50% of tumors with BGP. 2 Yanai et al 6 suggested that the BGP originated from the ILNR of the pelvis. The extension of BGP as an ILNR from a genuine WT could be explained by the known location of ILNR inside the renal lobules that thus could expand in the collecting system and the renal pelvis by itself with no concomitant WT extension, on the contrary of perilobar nephrogenic rests that are always located adjacent to the peripheral margin of the renal lobule, and directly expand in the cortex.…”
Section: Discussionmentioning
confidence: 99%
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“…Such examples include 'fetal rhabdomyomatous WT', 6 'botryoid WT', and 'teratoid WT'-however, these 'entities' do not exist in either of the two major classifications (SIOP and COG), 1,7 and these features are of no prognostic significance, so their usage is not recommended. 8,9 H…”
Section: Viable Tumour Componentsmentioning
confidence: 99%