| Literature DB >> 27134883 |
Pankaj Halder1, Bedabrata Mukhopadhyay2, Chhanda Das3, Madhumita Mukhopadhyay4.
Abstract
Pancreatoblastoma, is rare exocrine malignant tumour of childhood. We are reporting a case of three-year-old child presented to our hospital suffering from vague abdominal pain for further examination and treatment. Clinical examination revealed only a palpable abdominal mass. CT Scan revealed a huge complex space occupying lesion 9.1x8.8x9.2cm with large central cystic degeneration and lobulated enhancing peripheral solid components with foci of calcification, seem to arise from body and tail regions of pancreas. Surgery was done and mass was removed. By histopathology and immunohistochemistry it was diagnosed as pancreatoblastoma. The prognosis is very good in paediatric age, lacking evidence of metastatic disease at first presentation. Therefore early diagnosis is needed for specific treatment. The case is being reported because of its rarity.Entities:
Keywords: Alphafetoprotein; Mesenteric cyst
Year: 2016 PMID: 27134883 PMCID: PMC4843269 DOI: 10.7860/JCDR/2016/15336.7413
Source DB: PubMed Journal: J Clin Diagn Res ISSN: 0973-709X