| Literature DB >> 17142218 |
Hong Chang1, Lin Xu, Qingling Mu.
Abstract
An extra-adrenal pheochromocytoma is known as a paraganglioma. This report describes a patient with a rare primary functioning hepatic paraganglioma that resulted in hypertension. Computed tomography showed a highly vascular lesion located in segment 6 of the liver; it measured 6 x 5.5 cm. A right hemihepatectomy was subsequently performed; this was followed by an uneventful recovery and the disappearance of hypertension. The imaging characteristics and therapeutic principles of this rare tumor were gleaned from a review of the literature. Identification of this malignant tumor or possible recurrence is difficult, so longterm follow-up is recommended.Entities:
Mesh:
Year: 2006 PMID: 17142218 DOI: 10.1007/bf02850323
Source DB: PubMed Journal: Adv Ther ISSN: 0741-238X Impact factor: 3.845