Extra-adrenal pheochromocytoma at the organ of Zuckerkandl: a case report and literature review

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 complicatio...

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Detalles Bibliográficos
Autores principales: Gill, Tarana, Adler, Kalie, Schrader, Alicia, Desai, Keyur, Wermers, Joshua, Beteselassie, Nebiyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5417627/
https://www.ncbi.nlm.nih.gov/pubmed/28491185
http://dx.doi.org/10.1016/j.radcr.2016.12.009
Descripción
Sumario: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.

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