Case report - Adrenal collision tumour composed of oncocytoma and pheochromocytoma
Adrenal collision tumours (ACTs) are rare clinical entities denoting separate coexisting tumours involving adrenal glands. Here, we report the clinical, radiological and pathohistological presentation of a 49-year-old patient with an ACT composed of oncocytoma and pheochromocytoma. Following the initial diagnostic procedure guided by suspicion of pheochromocytoma, the patient has undergone surgery, recovered well and has been followed since. In the resected mass, oncocytoma was an incidental finding, as is typical of this type of tumour. With both components of this particular ACT being rare, this is a reminder of a need for widening differential diagnostic options when evaluating the patient for adrenal masses of unknown origin.
Authors
- Vladan Vukomanovic (ORCID: https://orcid.org/0000-0001-7197-5794)
- Predrag Savic
- Miloš Petrović (ORCID: https://orcid.org/0000-0002-2460-7793)
- R Zívić (ORCID: https://orcid.org/0000-0002-5124-2697)
- Sanja Ilic
- Jovana Lukic
- Stefan Mitic
Institutions
- University of Belgrade (RS)
- University Hospital Center Dr Dragiša Mišović (RS)
Publication Details
- Journal
- Frontiers in Oncology
- Published
- 2025-08-08
- DOI
- https://doi.org/10.3389/fonc.2025.1554355
- Primary Topic
- Adrenal and Paraganglionic Tumors
- Type
- article
- Field-Weighted Citation Impact
- 0.00