PARAGANGLIOMA: A CASE REPORT

Journal Title: Journal of Evidence Based Medicine and Healthcare - Year 2016, Vol 3, Issue 5

Abstract

INTRODUCTION Paragangliomas are relatively rare endocrine tumours that arise from paraganglionic tissue, a widely dispersed collection of specialized neural crest cells. In the absence of histological diagnosis and symptoms of catecholamine excess, paragangliomas may be mistaken for GISTs. Approximately, 50 cases of non-functional retroperitoneal paragangliomas were reported in the literature. We report a case of paraganglioma of the duodenum, which emphasizes the necessity to include extra-adrenal paraganglioma in the differential diagnosis and management of retroperitoneal tumors.

Authors and Affiliations

Aditya Date, Bharat Khadav, Mackson Nongmaithem

Keywords

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  • EP ID EP232034
  • DOI 10.18410/jebmh/2016/41
  • Views 96
  • Downloads 0

How To Cite

Aditya Date, Bharat Khadav, Mackson Nongmaithem (2016). PARAGANGLIOMA: A CASE REPORT. Journal of Evidence Based Medicine and Healthcare, 3(5), 173-175. https://europub.co.uk/articles/-A-232034