Table 4.
Elements of a focused history and physical examination are tailored towards detecting possible etiologies for an adrenal incidentaloma
Condition | History | Physical exam |
---|---|---|
Hypercortisolism (Cushing’s s yndrome) | Weight gain, central obesity, easy bruising, severe hypertension, diabetes, proximal muscle weakness, fatigue, depression, sleep disturbances, menstrual irregularities and virilization (in females), or fragility fractures | Hypertension, central obesity, supraclavicular fat accumulation, a dorsocervical fat pad, facial plethora, thinned skin, purple and wide (>1 cm) striae, acne, ecchymoses, hirsutism, and proximal muscle weakness or wasting |
Aldosteronism | Hypertension, hypokalemia, muscle cramping and weakness, headaches, intermittent or periodic paralysis | Hypertension, fluid retention |
Pheochromocytoma | Headaches, anxiety attacks, sweating, palpitations, or family history of von Hippel-Lindau disease, multiple endocrine neoplasia type 2, familial paraganglioma syndrome, or neurofibromatosis type 1 | Severe hypertension, tachycardia, arrhythmias, congestive heart failure, excessive sweating, anxiety, and pallor |
Adrenocortical c arcinoma | Flank pain, vague abdominal discomfort, hypercortisolism, virilization, feminization or aldosteronism | Weight loss, hirsutism, gynecomastia, signs of hypercortisolism |
Metastasis | Personal and family history of malignant lesions, weight loss, unexplained fevers, lack of adherence to an age-appropriate cancer screening program, and smoking history | Lymphadenopathy, lung mass, breast mass, renal mass or skin lesion suspicious for melanoma, as well as other cancer-specific findings |