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Titlebook: Medullary Thyroid Carcinoma; Friedhelm Raue Book 1992 Springer-Verlag Berlin Heidelberg 1992 Calcitonin.Karzinom.Medullary Thyroid Carcino

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發(fā)表于 2025-3-21 19:01:27 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書(shū)目名稱Medullary Thyroid Carcinoma
編輯Friedhelm Raue
視頻videohttp://file.papertrans.cn/631/630033/630033.mp4
叢書(shū)名稱Recent Results in Cancer Research
圖書(shū)封面Titlebook: Medullary Thyroid Carcinoma;  Friedhelm Raue Book 1992 Springer-Verlag Berlin Heidelberg 1992 Calcitonin.Karzinom.Medullary Thyroid Carcino
描述Medullary Thyroid Carcinoma is a rare thyroid tumororiginating from neural crest cells, the C-cell that impliesseveral special features, secretion of differentneuroendocrine markers, association with otherendocrinetumors and familial appearance. The familial variantofmedullary thyroid carcinoma allows an early detection bybiochemical and genetic testing. At that stage acceptablesurgical treatment will curethe patient. The sporadic formof medullary thyroid carcinoma will be diagnosed in aprogressive stage, but adequate surgical procedure can curethese patients too. Long term survival depends on stage,age, sex, and variant of the disease and seems to be as goodas in otherdifferentiated thyroid cancers.
出版日期Book 1992
關(guān)鍵詞Calcitonin; Karzinom; Medullary Thyroid Carcinoma; Medull?res Schilddrüsenkarzinom; Multiple Endocrine N
版次1
doihttps://doi.org/10.1007/978-3-642-84749-3
isbn_softcover978-3-642-84751-6
isbn_ebook978-3-642-84749-3Series ISSN 0080-0015 Series E-ISSN 2197-6767
issn_series 0080-0015
copyrightSpringer-Verlag Berlin Heidelberg 1992
The information of publication is updating

書(shū)目名稱Medullary Thyroid Carcinoma影響因子(影響力)




書(shū)目名稱Medullary Thyroid Carcinoma影響因子(影響力)學(xué)科排名




書(shū)目名稱Medullary Thyroid Carcinoma網(wǎng)絡(luò)公開(kāi)度




書(shū)目名稱Medullary Thyroid Carcinoma網(wǎng)絡(luò)公開(kāi)度學(xué)科排名




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Epidemiology of Medullary Thyroid Carcinoma second variant, MEN 2B, consists of MTC, pheochromocytoma, neural tumors, and a marfanoid habitus. The third variety of MTC is the non-MEN familial MTC, a hereditary MTC without any other endocrinopathies.
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Postsurgical Follow-Up and Managementth normal basal and pentagastrin-stimulated CT levels suggest a tumor-free state where no further treatment is necessary. They can then be followed-up at half-year intervals with physical examinations, and once a year a pentagastrin stimulation test has to be done (Grauer et al. 1990).
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