Extract

A 67-yr-old woman with an adrenal incidentaloma was diagnosed with ACTH-independent Cushing’s syndrome (urinary free cortisol = 286 μg/24 h; normal range, 25–90). She also had high plasma deoxycorticosterone, 11-deoxycortisol, and testosterone levels—findings suggestive of an adrenocortical carcinoma.

Computed tomography imaging showed a heterogeneous right adrenal mass (38 × 44 mm) with two components that had high and low attenuation densities for the upper and lower aspects, respectively (Fig. 1A).

Positron emission tomography (PET) scanning with 18F-fluorodeoxyglucose (FDG) and a [6β-131I]iodomethyl-19 nor-cholesterol (NP-59) scintigraphy showed a mirror image of the two components, suggesting a malignant upper tumor and a benign lower tumor, both of adrenocortical origin (Fig. 1, B and C).

Pathology confirmed the anticipated natures of the two different components: the upper one was an adrenocortical carcinoma (Weiss score = 7), and the lower one was an adrenocortical adenoma (Weiss score = 2) (Fig. 2).

Previous cases have documented the presence of a double component in adrenocortical tumors (1, 2), suggesting a multistep adrenal tumorigenesis. Recently, we showed that 18F-FDG PET helped distinguish between benign and malignant adrenal lesions (3).

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