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Adrenal Cortical Adenoma

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Atlas of Endocrine Pathology

Part of the book series: Atlas of Anatomic Pathology ((AAP))

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Abstract

Adrenal cortical adenomas are benign neoplasms of adrenal cortical cells that may or may not have functional activity. Adrenal cortical adenomas usually are single unilateral tumors that are more common in females. The incidence is unclear, particularly because many are identified as incidentalomas. Nonfunctional tumors often are identified as incidentalomas or in autopsies. A nonfunctional adrenal cortical adenoma may be associated with clinical symptoms if it is associated with hemorrhage or reaches a large size, although this is uncommon. Functional tumors may be associated with cortisol production (Cushing syndrome), aldosterone production (Conn syndrome), or sex steroid–producing tumors (virilization or feminization). Feminizing or virilizing tumors are quite uncommon, and the presence of these features is concerning for malignancy. Adrenal cortical adenomas may show degenerative features, hemorrhage, and cystic change.

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Erickson, L.A. (2014). Adrenal Cortical Adenoma. In: Atlas of Endocrine Pathology. Atlas of Anatomic Pathology. Springer, New York, NY. https://doi.org/10.1007/978-1-4939-0443-3_23

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  • DOI: https://doi.org/10.1007/978-1-4939-0443-3_23

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  • Publisher Name: Springer, New York, NY

  • Print ISBN: 978-1-4939-0442-6

  • Online ISBN: 978-1-4939-0443-3

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