PARAGANGLIOMA: A CASE REPORT

Abstract

Aditya Date1, Bharat Khadav2, Mackson Nongmaithem3

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.

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