| Literature DB >> 23583162 |
Shohei Honda1, Tadao Okada, Hisayuki Miyagi, Masatsugu Minato, Hiromu Suzuki, Akinobu Taketomi.
Abstract
Pancreatoblastoma is a rare pancreatic tumor that is most commonly encountered in infants and young children. This report describes an unusual presentation of a large pancreatic body pancreatoblastoma presenting with intraabdominal bleeding due to spontaneous rupture of the tumor in a 5-year-old boy. Subsequent molecular analysis from the resected specimen identified a mutation in CTNNB1 and aberrant methylation of the tumor suppressor RASSF1A.Entities:
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Year: 2013 PMID: 23583162 DOI: 10.1016/j.jpedsurg.2013.02.038
Source DB: PubMed Journal: J Pediatr Surg ISSN: 0022-3468 Impact factor: 2.545