Nicholas A. Tritos, Beverly M.K. Biller
rompt control of hypercortisolism is needed to reverse clinical and biochemical man- ifestations and decrease excess morbidity and mortality in patients with endogenous Cushing’s syndrome (CS).
Resection of the underlying tumor is currently the mainstay of treatment of CS.
After trans-sphenoidal pituitary surgery, persistent or recur- rent hypercortisolism may occur in, respectively, 10% to 20% and 20% to 30% of patients with pituitary corticotroph adenomas (ie, Cushing’s disease [CD]), which
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