Literature DB >> 1849635

Congenital hepatoblastoma and Beckwith-Wiedemann syndrome: a case study including DNA ploidy profiles of tumor and adrenal cytomegaly.

R Orozco-Florian1, J A McBride, B E Favara, A Steele, S J Brown, P Steele.   

Abstract

A case of fatal congenital hepatoblastoma is described in which the autopsy provided the first evidence of Beckwith-Wiedemann syndrome. Aneuploid quantitative DNA patterns were found by image analysis of the tumor and the cytomegalic adrenal gland.

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Year:  1991        PMID： 1849635     DOI： 10.3109/15513819109064749

Source DB:  PubMed          Journal:  Pediatr Pathol        ISSN： 0277-0938


  4 in total

1.  Neonatal hepatoblastoma in a newborn with severe phenotype of Beckwith-Wiedemann syndrome.

Authors:  Alessandro Mussa; Giovanni Battista Ferrero; Barbara Ceoloni; Eleonora Basso; Nicoletta Chiesa; Agostina De Crescenzo; Ernesto Pepe; Margherita Silengo; Luisa de Sanctis
Journal:  Eur J Pediatr       Date:  2011-03-30       Impact factor: 3.183

2.  DNA ploidy abnormalities in the liver of children with hereditary tyrosinemia type I. Correlation with histopathologic features.

Authors:  C Zerbini; D S Weinberg; K A Hollister; A R Perez-Atayde
Journal:  Am J Pathol       Date:  1992-05       Impact factor: 4.307

3.  Activin induces x-zone apoptosis that inhibits luteinizing hormone-dependent adrenocortical tumor formation in inhibin-deficient mice.

Authors:  Felix Beuschlein; Brendan D Looyenga; Stephanie E Bleasdale; Chris Mutch; David L Bavers; Albert F Parlow; John H Nilson; Gary D Hammer
Journal:  Mol Cell Biol       Date:  2003-06       Impact factor: 4.272

4.  The cell type-specific IGF2 expression during early human development correlates to the pattern of overgrowth and neoplasia in the Beckwith-Wiedemann syndrome.

Authors:  F Hedborg; L Holmgren; B Sandstedt; R Ohlsson
Journal:  Am J Pathol       Date:  1994-10       Impact factor: 4.307
  4 in total

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