Year: 2025
Type: article
Study design: Case Report
Abstract: 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.
Source: Frontiers in Oncology
Authors: Jovana Lukic, Sanja Ilic, Rastko Zivic, Stefan Mitic, Predrag Savic, Vladan Vukomanovic, Milos Petrovic
Language: English
Subfield: Surgery
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $3,801
OpenAlex ID: W4413255124