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2020, Number 6

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AMC 2020; 24 (6)

Carcinoid tumor of the duodenum: a rare and interesting incidental finding

Piamo-Morales AJ, Ferrer-Marrero D, Chávez-Jiménez D, Wilson-Batista E
Full text How to cite this article

Language: Spanish
References: 24
Page: 880-890
PDF size: 652.09 Kb.


Key words:

carcinoid tumor/diagnosis, duodenum/pathology, endosonography, case reports, neuroendocrine tumors/diagnosis.

ABSTRACT

Background: duodenal carcinoid tumor is rare; it represents 2 % of gastrointestinal neuroendocrine tumors. Therefore, a case of this is presented, recently diagnosed at the Joaquín Albarrán Clinical Surgical Hospital in Havana.
Objective: to report a case of carcinoid tumor of the duodenum and review the literature with emphasis on the histopathological diagnosis.
Clinical case: 86-year-old male patient who died on the fifth day after admission. At autopsy, during the macroscopic examination of the intestines, a lesion was revealed at the level of the first portion of the duodenum which, due to its histopathology, corresponded to a carcinoid tumor of the duodenum.
Conclusions: duodenal carcinoid is a rare tumor whose endoscopic or histological diagnosis is made incidentally in the vast majority of cases; it is generally associated with a benign progression, although endoscopic removal of tumors smaller than 1 cm without periampullary location or evidence of invasion of the muscular layer is recommended, evaluated by histology or endoscopic ultrasound.


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AMC. 2020;24