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Journal of Surgical Pathology and Diagnosis

ISSN: 2684-4575

Open Access

Volume 4, Issue 1 (2022)

Case Report Pages: 1 - 4

Atypical Carcinomatosis of Intestinal Neuroendocrine Tumor: Case Report and Literature Review

Jad Al Bitar, Souad Ghattas, Saleem Abdel Backi*, Omar Tabbikha, Colette Hanna and Raja Wakim

DOI: 10.37421/2684-4575.22.04.113

Neuroendocrine tumours are rare and slow growing neoplasms. They can grow and occur anywhere in the human body; however, the gastrointestinal system is the most common site. In our article we discuss a case of a 38-year-old male patient, who is previously healthy, and presented to our hospital after been complaining of left Para-umbilical and suprapubic pain of few weeks’ duration. CT abdomen pelvis with IV contrast was done in a peripheral hospital showing multiple abdominal cystic masses along with a variety of adenopathies of different sizes. Our general surgery team was consulted for surgical biopsy. Intra-op, the largest jejunal mass was identified, as well as, numerous abdominal adenopathies, mesenteric and peritoneal deposits suggestive of carcinomatosis. Pathology result came back conclusive of gastrointestinal neuroendocrine tumors.

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