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- W4382137684 abstract "The rectal neuroendocrine tumor (RNT) is a rare neoplasm that initiates in the neuroendocrine cells of the digestive tract called Kulchitsky cells, which originate from Lieberkün crypts. About 50% of patients are asymptomatic and their diagnosis is made incidentally by routine colonoscopies. This clinical report presents a neoplasm considered rare in a young patient and emphasizes the importance of its early diagnosis. A 23-year-old man, without comorbidities, was referred to the referral service to investigation a single occurrence of postprandial abdominal pain in the left flank. Polypoid fragment of the rectal mucosa was extracted during a colonoscopy, making it possible to perform a complete removal with free margins of the rectal NET. After histopathological and immunohistochemical evaluation, the diagnosis of RNT grade 1 was made. Although RNT is rare and asymptomatic, early screening is necessary to facilitate diagnosis in the early stage of the disease, leading to a greater possibility of treatment and a better prognosis of the disease." @default.
- W4382137684 created "2023-06-27" @default.
- W4382137684 creator A5092272114 @default.
- W4382137684 date "2021-01-01" @default.
- W4382137684 modified "2023-09-25" @default.
- W4382137684 title "Rectal Neuroendocrine Tumor: Clinical Case Report" @default.
- W4382137684 doi "https://doi.org/10.23880/oajco-16000173" @default.
- W4382137684 hasPublicationYear "2021" @default.
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