Massive paraganglioma masquerading as ovarian tumor: A unique case of paraganglioma of undetermined genetic origin
Paraganglioma and pheochromocytoma are rare tumors originating from chromaffin cells: pheochromocytoma from within the adrenal gland and paraganglioma from the sympathetic chain in the retroperitoneum. Though many are clinically silent, both classically present with hyperadrenergic symptoms. We present a case of a patient with an immense retroperitoneal mass found to be a clinically silent paraganglioma. The unusual size and presentation of the tumor as well as its undetermined genetic origin give a unique perspective into this rare tumor.
Authors
- Jacob Lucas
- Daniel C. Edwards (ORCID: https://orcid.org/0000-0002-4978-7460)
- S.S. Deshpande
- Oliver Gibb
Institutions
- Drexel University (US)
Publication Details
- Journal
- Baylor University Medical Center Proceedings
- Published
- 2025-01-16
- DOI
- https://doi.org/10.1080/08998280.2024.2448639
- Primary Topic
- Adrenal and Paraganglionic Tumors
- Type
- article
- Field-Weighted Citation Impact
- 0.00