Composite Pheochromocytoma-Paraganglioma With Ganglioneuroma: A Dual-Center Clinical Experience
Patients with PPGL-GN were younger and had a higher occurrence of underlying genetic disorders compared to PHEO. However, PPGL-GN was radiologically indistinguishable from PHEO. The higher observed disease recurrence of PPGL-GN reinforces vigilant postoperative follow-up.
Authors
- Sarah C. Oltmann (ORCID: https://orcid.org/0000-0002-7180-4167)
- Oksana Hamidi (ORCID: https://orcid.org/0000-0002-7367-3885)
- Fiemu E. Nwariaku
- Hussam Alkaissi (ORCID: https://orcid.org/0000-0002-0861-9348)
- Karel Pacák (ORCID: https://orcid.org/0000-0002-3541-3767)
- Shubham Agarwal (ORCID: https://orcid.org/0000-0002-7981-9603)
- Liwei Jia (ORCID: https://orcid.org/0000-0002-2118-6428)
- J. Izurieta
- Mary Grace Roden
- Alan P.B. Dackiw
Institutions
- National Institutes of Health (US)
- University of Utah (US)
- National Institute of Diabetes and Digestive and Kidney Diseases (US)
- Université Bourgogne Franche-Comté (FR)
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (US)
- The University of Texas Southwestern Medical Center (US)
Publication Details
- Journal
- Journal of the Endocrine Society
- Published
- 2025-02-26
- DOI
- https://doi.org/10.1210/jendso/bvaf036
- Citations
- 1
- Primary Topic
- Adrenal and Paraganglionic Tumors
- Type
- article
- Field-Weighted Citation Impact
- 2.01
Funders
- University of Texas Southwestern Medical Center