The clinically inapparent adrenal mass: update in diagnosis and management.
By G. Mansmann, Joseph Lau, E. Balk, M. Rothberg, Y. Miyachi, S. Bornstein. Endocrine reviews, 2004
782 citations recorded by the source corpus.
Subfields: Cancer Research, Endocrinology, Diabetes and Metabolism, Surgery
View Paper: https://www.semanticscholar.org/paper/fe8c9a716260ef1da329d4e56a1da15d7c2400ab
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Citations in the corpus
- Managing incidental findings on abdominal CT: white paper of the ACR incidental findings committee. (2010, background): “The most frequent pathology for an incidentally iscovered adrenal mass is a nonhyperfunctioning adeoma [64].”
- Pheochromocytoma and paraganglioma: an endocrine society clinical practice guideline. (2014, background): “Nearly 5% of patients with incidentally discovered adrenal masses on anatomical imaging prove to have a pheochromocytoma (13, 14).”
- Clinical review: The pathogenetic role of cortisol in the metabolic syndrome: a hypothesis. (2009, background): “These lesions are characterized by autonomous glucocorticoid production without signs or symptoms of CS (48).”
- American Association of Clinical Endocrinologists and American Association of Endocrine Surgeons Medical Guidelines for the Management of Adrenal Incidentalomas: executive summary of recommendations. (2009, neutral): “Review of the literature reveals no level of evidence stronger than level 2 to support recommendations for the management of patients with pheochromocytoma (44 [EL 4]) .”