Literature DB >> 3962517

Pancreoblastoma in a neonate associated with Beckwith-Wiedemann syndrome.

S R Potts, S Brown, M D O'Hara.   

Abstract

A cystic abdominal mass was removed from a male child born at 32 weeks gestation. Histological examination showed this to be a pancreoblastoma. Both clinical and histological features of Beckwith-Wiedemann syndrome developed within the first 12 weeks of life. The child remains well and thriving with no tumour recurrence at 10 months of age.

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Year:  1986        PMID: 3962517     DOI: 10.1055/s-2008-1043310

Source DB:  PubMed          Journal:  Z Kinderchir        ISSN: 0174-3082


  4 in total

1.  Beckwith-Wiedemann syndrome, pancreatoblastoma, and the wnt signaling pathway.

Authors:  Natalie J Kerr; Ryuji Fukuzawa; Anthony E Reeve; Michael J Sullivan; Ryuji Fukazawa
Journal:  Am J Pathol       Date:  2002-04       Impact factor: 4.307

2.  A case of pancreatoblastoma prenatally diagnosed as intraperitoneal cyst.

Authors:  Michihiro Sugai; Norihisa Kimura; Minoru Umehara; Hirohumi Munakata; Nobuhisa Yajima; Soroku Yagihashi; Gunther Klöppel
Journal:  Pediatr Surg Int       Date:  2006-08-01       Impact factor: 1.827

Review 3.  Wiedemann-Beckwith syndrome.

Authors:  W Engström; S Lindham; P Schofield
Journal:  Eur J Pediatr       Date:  1988-06       Impact factor: 3.183

4.  Pancreatoblastoma in an adult: its separation from acinar cell carcinoma.

Authors:  A Hoorens; F Gebhard; K Kraft; N R Lemoine; G Klöppel
Journal:  Virchows Arch       Date:  1994       Impact factor: 4.064

  4 in total

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