ECE2018 Poster Presentations: Adrenal and Neuroendocrine Tumours Adrenal cortex (to include Cushing's) (70 abstracts)
1Division of Endocrinology and Centre for Applied Biomedical Research, Department of Medical and Surgical Sciences, Alma Mater Studiorum, University of Bologna, Bologna, Italy; 2Operative Unit of Pathology, St Orsola Malpighi Hospital, Bologna, Italy; 3Diagnostic and Interventional Radiology Unit, Department of Diagnostic and Preventive Medicine, St Orsola-Malpighi Hospital, Bologna, Italy; 4Divison of Nuclear Medicine, St Orsola-Malpighi Hospital, Bologna, Italy; 5Division of General Surgery, Department of Medical and Surgical Sciences, Alma Mater Studiorum, University of Bologna, Bologna, Italy.
Background: Up to 30% of incidentally-discovered adrenal masses are lipid-poor adenomas (LPA). The clinical significance of LPA is poorly understood. The aim of the study was to investigate histopathological features of LPA and their association with radiological parameters.
Methods: A total of 39 patients with radiological evidence of LPA were included. LPA was defined as an adrenal mass with pre-contrast Hounsfield units (HU) ≧10, associated with absolute washout >60% or relative washout >40% after contrast infusion. Patients underwent hormonal work-up for primary aldosteronism (aldosterone/plasma renin activity ratio >30 in orthostatic position and after Captopril test) and pheochromocytoma (elevated urinary metanephrines). Hypercortisolism was defined as cortisol levels after 1 mg-dexamethasone suppression test >50 nmol/l. F18-Fluoro-Deoxy-Glucose (FDG)-PET scan was performed in 31/39 patients. In resected tumors, Weiss, Lin-Weiss-Bisceglia, and PASS score were calculated, where appropriate.
Results: Radiological characteristics of the population were as follows (mean±SD): tumor diameter 23.0±10.9 mm, pre-contrast density 27.5±10.2HU, absolute and relative washout 68.1±7.6% and 50.7±7.5%, respectively, and FDG-PET scan 6.1±4.6 SUV. Hormonal evaluation showed Cushings syndrome in 7/39 patients (18%), subclinical hypercortisolism in 11/39 subjects (28%), primary aldosteronism in 2/39 patients (5%) and elevated metanephrines in 2/39 subjects (5%). The remaining cases (17/39, 44%) were non-secreting. Eighteen patients underwent adrenalectomy because of tumor diameter (n=2), hormonal hypersecretion (n=9) and high FDG-PET SUV (n=7). Histopathological examination showed adrenocortical adenoma in 12/18 cases (66%) and adrenocortical carcinoma in 3/18 tumors (17%), as defined by Weiss score. Hemangioma was diagnosed in 1/18 cases. The two remaining tumors were pheochromocytoma (PASS score 3 and 7). Among all adrenocortical tumors, abundant granular eosinophilic cytoplasm was found in 11/15 cases (73%). By applying the Lin-Weiss-Bisceglia score, one tumor was confirmed malignant, whereas 3/11 tumors were borderline. Weiss score was positively associated with pre-contrast density (Odds Ratio [OR] 1.088, 95% Confidence Interval (CI) 1.0181.163, P=0.013) and absolute washout (OR 1.105, 95%CI 1.0051.216, P=0.039). Lin-Weiss-Bisceglia score was positively associated with tumor diameter (OR 1.045, 95%CI 1.0151.076, P=0.003) and pre-contrast density (OR 1.046, 95%CI 1.0021.091, P=0.039).
Conclusion: LPA represents a heterogeneous class of tumors, which may include pheochromocytoma and adrenocortical carcinoma. In our pilot study, 5/18 (28%) LPAs were classified as malignant or borderline at histopathological analysis. Eosinophilic cytoplasm is a common finding in those tumors and Lin-Weiss-Bisceglia score may be used to avoid overdiagnosis of malignancy.