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Minority are functional, may produce a pure or mixed endocrine syndrome (from most to
least common):
Hyperaldosteronism/Conn’s syndrome: hypertension, proximal muscle weakness,
headache, polyuria, tachycardia with/without palpitation, hypokalemia, hypocalcemia
Hypercortisolism/Cushing’s syndrome: central obesity, moon facies, plethora, striae,
thin skin, easy bruising, hirsutism, telangiectasias, hyperhidrosis
Virilization:
Females: increased muscle mass (Herculean habitus), clitoromegaly, facial hair, deep
voice, pubic hair
Males: penile enlargement, pubic hair
Feminization: gynecomastia, impotence
Well-circumscribed lesion comprised of cells resembling any of the 3 layers of the normal
adrenal cortex
Difficult to differentiate ACA from normal adrenal cortex in adrenal core needle biopsies
Computed tomography (CT):
Rounded, well delineated borders, homogeneous, clear separation from and no extension
into surrounding structures, decreased attenuation compared to uninvolved adrenal
parenchyma on non-contrast CT (≤10 HU), contrast enhancing (Theranostics 2012;2:516)
Magnetic resonance imagining (MRI):
Used to visualize microscopic fat (favoring ACA), “chemical shift” phenomenon (increased
“in phase” signal intensity, decreased “out of phase” signal) (Theranostics 2012;2:516)
18FDG-PET:
Malignant lesions have greater 18FDG uptake than liver (Theranostics 2012;2:516)