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Titlebook: Diagnosis and Management of Endocrine-related Tumors; Richard J. Santen (Professor of Medicine, Chief),A Book 1984 Martinus Nijhoff Publis

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The syndrome of multiple endocrine neoplasia type I, of individual patients with solitary endocrine tumors has prompted the subsequent elucidation of extensive pedigrees which manifest pluriglandular tumors over several generations. Conversely, the prior identification of a kindred with established multiple endocrine tumors has permitted the timely r
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Prolactin secreting pituitary adenomas in women,ing were in fact secreting PRL. Of all pituitary tumors those secreting PRL account for approximately 50–55%. Thus PRL secreting pituitary tumors or prolactinomas are becoming a commonly encountered disease rather than a medical curiosity.
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Endocrine neoplasms: carcinomas of the thyroid,tumor’s growth truly important for progress in successfully dealing with thyroid cancers. From this perspective we will discuss the four most common cancers of the thyroid, emphasizing shortcomings and limitations in our current therapy and goals for improved future management.
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Adrenocortical tumors,t may be diagnosed more with the increasing use of CT scans [4, 5], particularly sector CT scans and abdominal ultrasound studies. Malignant nonfunctional tumors are also very infrequent, comprising only about 0.2% of all reported carcinomas [6].
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The syndrome of multiple endocrine neoplasia type I,mors over several generations. Conversely, the prior identification of a kindred with established multiple endocrine tumors has permitted the timely recognition and detection of emerging neoplasms in other family members at genetic risk.
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Handwörterbuch Arbeitsbeziehungen in der EGpersecretion of prolactin [1], growth hormone [2], and ACTH [3] due to a functioning pituitary adenoma. As it might be expected, the success of the surgery has been found to be inversely related to the size of the tumor, with the best results obtained in patients with microadenomas (i.e. <10 mm in diameter).
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