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  • Title: Cecal carcinoid tumor in a nigerian man: A case report and review of literature.
    Author: Obateru OA, Taiwo JA, Oladejo S, Awelimobor DA, Fadaunsi OO, Olokoba AB.
    Journal: Niger J Clin Pract; 2017 May; 20(5):634-636. PubMed ID: 28513526.
    Abstract:
    Carcinoid tumors are rare neuroendocrine tumors that have been reported in a wide range of organs but most commonly involve the gastrointestinal tract (stomach, ileum, appendix, and colon), and rarely ovary and thymus. We present a case of a 56-year-old Nigerian man with a cecal carcinoid tumor that was surgically removed. A 56-year-old Nigerian man, presented to our hospital with a year history of right-sided lower abdominal fullness, audible bowel sounds, occasional diarrhea, nausea, vomiting, and epigastric pain. There was no history of hematochezia or passage of melena stool. Colonoscopy revealed a cecal mass occupying more than two-thirds of the cecal lumen. Histology confirmed carcinoid tumor (well-differentiated neuroendocrine tumor), which was surgically removed. Carcinoid tumors are slow growing rare neuroendocrine tumors. Mortality is low if it is diagnosed early.
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