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Titlebook: Endocrine Neoplasms; Andrew Arnold (Chief, Associate Professor of Medic Book 1997 Springer Science+Business Media Dordrecht 1997 Tumor.can

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Book 1997crine neoplasms. This is therefore an excellent point at which to undertake a broad­ based overview of the state of the art in endocrine neoplasia for the Cancer Treatment and Research series. Because of the wide and interdisciplinary readership of this series, our aim for each chapter has been to p
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Follicular cell-derived thyroid carcinomas,from tumors elsewhere. Besides being extremely rare, all of the latter, with the exception of medullary thyroid carcinoma, are tumors derived from nonendocrine tissues, and therefore they are not the subject of this review. Medullary thyroid carcinoma is covered in Chapter 20.
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Parathyroid carcinoma,sm, and when recurrences eventually occur they are predominantly located cervically. This fact may initially lead the surgeon to assume that the tumor is not malignant. The term . was coined for borderline lesions with a clinically benign course [1].
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David A. Edelman,Gary S. Berger,Louis Keithtulated that the tumor released a parathyroid hormone (PTH)-like factor that could not only stimulate bone resorption but could also induce phosphaturia, leading to hypophosphatemia. The concept of . or . as a cause of hypercalcemia in malignancy (HM) was thus born.
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