Literature DB >> 24057473

Neuroblastoma arising from the celiac ganglion.

F Ito1, T Ito, H Ando, T Seo.   

Abstract

Neuroblastoma from the celiac ganglion (CG) is rare, accounting for only 1.4% (2 out of 144 cases) of all neuroblastomas. This is a case report of two infants with neuroblastoma from the CG detected by mass screening. Imaging techniques revealed a tumor in front of the aorta with involvement of the celiac axis and its main branches, which was confirmed at operation. Although incision of the tumour capsule was required to preserve the vessels, the outcome of these patients was good with disease-free survival of 2 and 12 years, respectively.

Entities:  

Year:  2013        PMID: 24057473     DOI: 10.1007/BF00174587

Source DB:  PubMed          Journal:  Pediatr Surg Int        ISSN: 0179-0358            Impact factor:   1.827


  3 in total

1.  A comparison of four staging systems for localized and regional neuroblastoma: a report from the Childrens Cancer Study Group.

Authors:  A E Evans; G J D'Angio; H N Sather; A A de Lorimier; A Dalton; R S Ungerleider; J Z Finklestein; G D Hammond
Journal:  J Clin Oncol       Date:  1990-04       Impact factor: 44.544

2.  The role of second-look procedures in the management of retroperitoneal tumors in children.

Authors:  J L Grosfeld; K W West; T R Weber
Journal:  Am J Pediatr Hematol Oncol       Date:  1984

3.  Long-term effects of mass screening for neuroblastoma in infancy.

Authors:  T Sawada; T Matsumura; H Kawakatsu; T Sugimoto; H Kuroda; H Hosoi; T Michihata; T Saida; T Hino
Journal:  Am J Pediatr Hematol Oncol       Date:  1991
  3 in total

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