Hormonal Evaluation
Hormonal evaluation in ACC is most practical when divided into the baseline adrenal workup for a suspicious mass, expanded steroid precursor and multisteroid profiling, and syndrome-specific testing for uncommon functional phenotypes.123
Diagnostic Map
Baseline Endocrine Workup for Suspected ACC
These papers cover the core hormone panel for an adrenal mass when ACC is possible, including cortisol autonomy, androgen excess, and exclusion of pheochromocytoma before intervention.123
Grouped note: Baseline Endocrine Workup for Suspected ACC
Steroid Precursor and Multisteroid Profiling in ACC
This cluster follows the shift from single-analyte testing to urinary or plasma steroid signatures, precursor excess, and mass-spectrometry-based profiling.123
Grouped note: Steroid Precursor and Multisteroid Profiling in ACC
Context-Specific Hormonal Syndromes in ACC
These reports focus on aldosterone-, estrogen-, or other atypical secretory states that require tailored biochemical interpretation.123
Grouped note: Context-Specific Hormonal Syndromes in ACC
How to Read This Literature
The grouped notes below move from mandatory triage testing to the more specialized biochemical tools that refine diagnosis and tumor biology.123
See Also
References
Footnotes
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Adrenocortical carcinomas and malignant phaeochromocytomas: ESMO-EURACAN Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann Oncol. 2020. PMID: 32861807. Local full text: 32861807.md ↩ ↩2 ↩3 ↩4 ↩5
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Adrenocortical carcinoma: a practical guide for clinicians. Lancet Diabetes Endocrinol. 2025. PMID: 40086465. Local full text: 40086465.md ↩ ↩2 ↩3 ↩4 ↩5
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Management of cushing’s syndrome in patients with adrenocortical cancer: state of the art and future perspectives. Rev Endocr Metab Disord. 2025. PMID: 40736645. Local full text: 40736645.md ↩ ↩2 ↩3 ↩4 ↩5