Gangliocytic paraganglioma: A rare cause of gastrointestinal bleeding

9Citations
Citations of this article
16Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Duodenal neuroendocrine tumors (NETs) are rare tumors, consisting of five different types of tumors. In many cases, they may be asymptomatic, leading to delay in diagnosis. Clinical symptoms are related to local tumor growth and mucosal ulceration. We report a 38-year old man with duodenal gangliocytic paraganglioma causing overt upper gastrointestinal bleeding and anemia. We describe specific clinical and histopathological features of the tumor, and review the diagnostic and therapeutic strategy. Gangliocytic paragangliomas are regarded as benign tumors. However, the disease recurrence and the malignant potential of the tumor have also been reported.

Cite

CITATION STYLE

APA

Boeriu, A., Dobru, D., Georgescu, R., Mocan, S., & Boeriu, C. (2015). Gangliocytic paraganglioma: A rare cause of gastrointestinal bleeding. Journal of Gastrointestinal and Liver Diseases, 24(1), 109–112. https://doi.org/10.15403/jgld.2014.1121.abo

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