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Titlebook: Medullary Thyroid Cancer; Tracy S. Wang,Douglas B. Evans Book 2016 Springer International Publishing Switzerland 2016 Prophylactic Thyroid

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The Physiology of Serum Calcitonin and Carcinoembryonic Antigen in Medullary Thyroid Cancer, the neural crest and predominantly secrete calcitonin, as well as several other hormones and amines, including carcinoembryonic antigen (CEA), adrenocorticotropic hormone (ACTH), β-melanocyte stimulating hormone, chromogranin, histaminase, neurotensin, and somatostatin [.–.]. Calcitonin is expresse
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Preoperative Evaluation of the Patient with Medullary Thyroid Cancer,uires the clinician to be familiar with the details of genetics, pathology, endocrinology, surgery, and radiology that specifically pertain to MTC. The purpose of this chapter is to summarize the current standard-of-care preoperative evaluation of the patient with MTC.
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Inherited Medullary Thyroid Carcinoma: Indications and Technique of Early Thyroidectomy,ble endocrine disease. Since the discovery of the role of activating mutations in the . proto-oncogene in MEN2A and MEN2B, considerable advances in management have occurred, and most of the asymptomatic . carriers who have undergone early thyroidectomy can lead full lives unencumbered by the presenc
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Surgical Management of Inherited MTC: Therapeutic Thyroidectomy,creening of at-risk family members can identify those who may benefit from prophylactic thyroidectomy, patients with de novo mutations or who have deferred screening can still present with clinically or biochemically evident MTC. Therapeutic total thyroidectomy with central compartment lymph node di
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Surgical Management of Parathyroid and Adrenal Glands in Inherited Medullary Thyroid Carcinoma,of the adrenal glands and parathyroid glands in classical MEN2A and MEN2B. Classical MEN2A is associated with pheochromocytoma and primary hyperparathyroidism, which both have varied frequency/penetrance depending on the specific RET mutation. In MEN2B pheochromocytoma will develop in approximately
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