| Literature DB >> 28138625 |
Peng Li1, Dongbing Zhao1.
Abstract
Paraganglioma is a rarely type of neuroendocrine neoplasm with the ability of neuropeptide and catecholamine secretion. Hypertension and sympathetic hyperactivity was the most common clinical presentation. And it is still a challenge to determine the biological behavior pathologically. Here, we reported a case of paraganglioma originated from retroperitoneal with the classical clinical presentation. Radical resection was performed successfully and malignant tendency was revealed in pathology. Meanwhile, literature review was conducted in order to figure out the diagnosis and prognosis.Entities:
Keywords: Paraganglioma; diagnosis; prognosis; surgery; treatment
Year: 2016 PMID: 28138625 PMCID: PMC5244753 DOI: 10.21037/tgh.2016.06.01
Source DB: PubMed Journal: Transl Gastroenterol Hepatol ISSN: 2415-1289