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Adrenal collision tumors (ACTs) are rare lesions in which two histologically distinct tumors coexist within the same adrenal gland. They are almost always incidental findings, and although their heterogeneous, dual-component appearance can raise concern for malignancy, they seldom represent a distinct clinical problem. The principal pitfall they create is radiologic rather than biochemical: the mixed composition of an ACT renders the adrenal CT washout protocol unreliable and can mimic a neoplasm. The established adrenal incidentaloma pathway (biochemical exclusion of pheochromocytoma and adrenocortical carcinoma, imaging phenotyping, and size- and growth-based surveillance) reliably identifies both a functional and a malignant component of a collision tumor . Drawing on institutional experience and the published case literature, this narrative review describes the entity and its imaging caveats, and shows how the standard pathway can be applied to risk-stratify low-risk lesions and avoid unnecessary surgery while selecting appropriate first-line imaging.
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Botros et al. (2026) studied this question.
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