Literature DB >> 31735130

Primary mesenteric neuroendocrine tumour with liver metastasis: a common presentation of an uncommon tumour.

Ambuj Agarwal1, Lileswar Kaman2, Ashish Gupta3, Krishna Ramavath1, Kim Vaiphei4.   

Abstract

Neuroendocrine tumours (NET) are rare. They usually arise from the gastrointestinal or bronchopulmonary systems. Most are discovered incidentally and the small bowel tumours pose special difficulty in detection and treatment. Primary mesenteric involvement is very rare. Here we report such a case with a liver metastasis. This was preoperatively diagnosed and treated by enucleation of the mesenteric tumour together with right hepatectomy in a single sitting.

Entities:  

Keywords:  Neuroendocrine tumour; chromogranin; liver metastasis; mesenteric neuroendocrine tumour

Mesh:

Year:  2019        PMID: 31735130     DOI: 10.1177/0049475519887657

Source DB:  PubMed          Journal:  Trop Doct        ISSN: 0049-4755            Impact factor:   0.731


  1 in total

1.  An apparent primitive mass of the mesentery: A case report.

Authors:  Antonio Costanzo; Marco Canziani; Cesare Carlo Ferrari; Valentina Bertocchi; Saro Cutaia; Eraldo Oreste Bucci; Elisabetta Uslenghi; Andrea Ferretti; Marco De Luca; Fabio Ceriani
Journal:  Medicine (Baltimore)       Date:  2022-06-17       Impact factor: 1.817

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.