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Objective: Currently, it is unclear whether pheochromocytomas can be ruled out based on low intensity on T2-weighted sequences and signal loss on out-of-phase magnetic resonance imaging (MRI) sequences. Hence, in this study, we investigated whether biochemical screening for pheochromocytoma in patients with adrenal incidentalomas (AIs) showing MRI features not suggesting pheochromocytoma would prove beneficial.
Methods: We performed MRI for 300 AIs in 278 consecutive patients. All patients were screened for pheochromocytoma with plasma metanephrine and normetanephrine. Patients with high plasma levels of metanephrine and/or normetanephrine were also assessed for pheochromocytoma by urinary metanephrines.
Results: Hyperintensity was detected on T2-weighted MRI sequences in 28 (9.3%) of the 300 AIs. Among these 28 incidentalomas, pheochromocytoma was diagnosed in 13 (46.4%) of the cases by histopathologic analysis. Hyperintensity on T2-weighted MRI was significantly higher in pheochromocytomas compared to the remaining AIs (P<.001). All 13 pheochromocytomas were characterized by hyperintensity on T2-weighted sequences and the absence of signal loss on out-of-phase MRI sequences. Pheochromocytoma was not detected in any of the 272 AIs that appeared hypointense or isointense on T2-weighted MRI sequences or in the 250 cases with signal loss on out-of-phase sequences.
Conclusion: The results of this study suggest that AIs that appear hypointense or isointense on T2-weighted MRI sequences and those with signal loss on out-of-phase sequences may not require routine biochemical screening for pheochromocytoma. Further studies including a higher number of pheochromocytomas are required to confirm our results.
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http://dx.doi.org/10.4158/EP151060.OR | DOI Listing |
Endocrine
September 2025
Grupo de Patología Adrenal AdrenoSEEN de la Sociedad Española de Endocrinología y Nutrición (SEEN), Madrid, Spain.
Endocrinol Diabetes Metab Case Rep
July 2025
Division of Endocrinology and Metabolism, Albany Medical College, Albany, New York, USA.
Summary: Pheochromocytomas are rare neuroendocrine tumors derived from adrenal chromaffin cells that result in hyperactivity of the sympathetic nervous system. We present the case of a patient with biochemical evidence of pheochromocytoma, but surgical pathology revealed absence of tumor. This is an 80-year-old female with a past medical history of metastatic follicular lymphoma and hypertension with an incidental 1.
View Article and Find Full Text PDFJ Endocrinol Invest
August 2025
Department of Medical Biotechnology and Translational Medicine, University of Milan, Milan, 20100, Italy.
Purpose: Cushing's syndrome (CS) is a rare condition marked by overt hypercortisolism, while mild autonomous cortisol secretion (MACS) refers to asymptomatic or subclinical cortisol excess, often associated with adrenal incidentalomas (AI). MACS is significantly more prevalent than CS, particularly in older populations. The 1 mg overnight dexamethasone suppression test (F-1mgDST) is the main diagnostic tool, but the appropriateness of its current cut-off value of 1.
View Article and Find Full Text PDFEur J Endocrinol
August 2025
Department of Medical and Surgical Sciences, Alma Mater Studiorum University of Bologna, 40138 Bologna, Italy.
Endocr Connect
September 2025
3rd Department of Internal Medicine, General University Hospital in Prague and The 1st Faculty of Medicine of Charles University, Prague, Czech Republic.
Introduction: The overnight dexamethasone suppression test (DST) is recommended for the initial testing of Cushing's syndrome. Simultaneous measurement of dexamethasone and cortisol is recommended. This study aimed to determine the cutoff value for dexamethasone measured in DST analyzed via liquid chromatography tandem mass spectrometry (2D-LC-MS/MS) and to assess whether analysis of adrenal steroids other than cortisol may improve diagnostic accuracy.
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