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The Surgical Management of Cushing’s Disease

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Cushing's Syndrome

Part of the book series: Contemporary Endocrinology ((COE))

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Abstract

The prompt and effective lowering of increased cortisol becomes essential for the well-being of patient’s with Cushing’s disease. As 80% of patients with the clinical signs and symptoms of Cushing’s disease have a pituitary source of excessive and uncontrolled adrenocorticotropic hormone (ACTH) secretion, well-trained pituitary surgeons are required to deal with this complex disease. At present, surgical removal of a pituitary adenoma which is the source of excessive ACTH provides the most reliable method of reducing cortisol, with the potential for “cure” of the tumor and immediate remission of disease. The most popular methods are endonasal microsurgical or endoscopic approaches, which have become increasingly safe and effective. The goals of surgery are to reverse the endocrinopathy and restore normal pituitary function; eliminate mass effect and restore normal neurological function; eliminate or minimize the possibility of tumor recurrence; and obtain a definitive histologic diagnosis. Reported long-term recurrence rates mandate close monitoring in this patient population.

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Dunn, I.F., Laws, E.R. (2010). The Surgical Management of Cushing’s Disease. In: Bronstein, M. (eds) Cushing's Syndrome. Contemporary Endocrinology. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-60327-449-4_10

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  • DOI: https://doi.org/10.1007/978-1-60327-449-4_10

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