Primary mesenteric carcinoid tumor

22Citations
Citations of this article
7Readers
Mendeley users who have this article in their library.

Abstract

Primary mesenteric carcinoid tumor is very rare, although secondary mesenteric involvement is common, reported as 40% to 80%. And distant metastasis rate reported as 80% to 90%, when the size is larger than 2 cm. We present a case of very rare primary mesenteric carcinoid tumor showing benign character though large size. The patient visited St. Vincent's Hospital, The Catholic University of Korea with increasing palpable abdominal mass. At laparotomy, a well encapsulated mass arising from the mesentery near the ligament of Treitz was found without any adjacent organ invasion or distant metastasis. The mass was measured as 8.2 × 7.3 cm and histopathologically benign character. At 11 months of follow up, the patient was recurrence free. Copyright © 2013, the Korean Surgical Society.

Author supplied keywords

Cite

CITATION STYLE

APA

Park, I. S., Kye, B. H., Kim, H. S., Kim, H. J., Cho, H. M., Yoo, C., & Hwang, S. S. (2013). Primary mesenteric carcinoid tumor. Journal of the Korean Surgical Society, 84(2), 114–117. https://doi.org/10.4174/jkss.2013.84.2.114

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free