Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8825429 | Radiology Case Reports | 2017 | 5 Pages |
Abstract
Pheochromocytomas and paragangliomas are tumors that occur in characteristic locations and are commonly detected on imaging studies. A correct diagnosis is important because of differences in associated neoplasms, risk for malignancy, and need for genetic testing. In addition, associated complications, including death, can be avoided if appropriately recognized and treated. Here, we report a rare case of an extra-adrenal paraganglioma of the organ of Zuckerkandl.
Related Topics
Health Sciences
Medicine and Dentistry
Radiology and Imaging
Authors
Tarana BA, Kalie DO, Alicia DO, Keyur BA, Joshua DO, Nebiyu MD,