| Literature DB >> 31735130 |
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