Cecal carcinoid tumor in a nigerian man: A case report and review of literature

Nigerian Journal of Clinical Practice
O A ObateruA B Olokoba

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.

References

Jun 1, 1985·American Journal of Surgery·J M Rosenberg, J P Welch
Sep 1, 1972·Diseases of the Colon and Rectum·R S Berardi
Feb 6, 2003·Cancer·Irvin M ModlinMark Kidd
Jun 24, 2004·Annals of Surgery·Melinda A MaggardClifford Y Ko
Mar 17, 2010·Arquivos De Gastroenterologia·Daniel Reis WaisbergJaques Waisberg
Jul 9, 2013·The Journal of Surgical Research·Sara E MurrayHerbert Chen

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