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Annali Italiani di Chirurgia 2016

Synchronous ileal neuroendocrine tumor: diagnosis and treatment. A case report and review of the literature.

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Antonino Buffone
Dario Cavallaro
Salvatore Lo Bianco
Lidia Puzzo
Pietro Caglià
Matteo Angelo Cannizzaro

キーワード

概要

BACKGROUND

The majority of neuroendocrine tumors (NET) are located in the gastrointestinal tract (67.5%) and in the bronchopulmonary (25.3%).

METHODS

CA, female, 42 years old, profuse diarrhea about two months, cramping for increased peristalsis, vomiting and weight loss. The patient, diagnosed with ileal neuroendocrine tumor, by colonoscopy with biopsy of lesion, therefore came in our unit to be subjected to surgical therapy. Plasma assay Chromogranin A was performed: 160 ng / ml (nv: 15-100 ng / ml). The patient underwent surgery of right hemicolectomy.

CONCLUSIONS

Neuroendocrine tumors although are rare diseases, have an increasing impact, probably by virtue of improved diagnostic methods. In case of profuse diarrhea should be suspected a neuroendocrine tumor. Certainly the diagnosis of certainty is given by histological examination (biopsy or resected nodule).

CONCLUSIONS

After surgical excision is necessary to perform the follow-up of chromogranin A, and, if not executed, perform nuclear medicine examinations such as Octreoscan and PET.

UNASSIGNED

Chromogranin A, Neuroendocrine tumor, Octreoscan.

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