1.
Journal of the Korean Pediatric Society
;
: 861-865, 1996.
Artigo
em Coreano
| WPRIM
| ID: wpr-32554
RESUMO
We experenced a case of cystic pancreatoblastoma associated with congenital hemihypertrophy in a 4 months old male. The mass was located on the anterior side of pancreatic head without any connection to the pancreas. After exision of cystic pancreatoblastoma, chemotherapy(FAM regimen) was performed 15 times due to capsular tumor invasion. Until this time there was no drug side effect and metastasis. The patient's general condition is stable.