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Titlebook: Management of rare adult tumours; Yazid Belkacémi (Professor Radiation Oncology, Dep Book 2010 Springer-Verlag Paris 2010 breast cancer.ca

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發(fā)表于 2025-3-21 18:03:41 | 只看該作者 |倒序瀏覽 |閱讀模式
書目名稱Management of rare adult tumours
編輯Yazid Belkacémi (Professor Radiation Oncology, Dep
視頻videohttp://file.papertrans.cn/623/622595/622595.mp4
概述A reference book on rare adult cancer management with the contribution of 70 experts.The knowledge comes from recent developments in molecular diagnostics, systemic treatments with new drugs and targe
圖書封面Titlebook: Management of rare adult tumours;  Yazid Belkacémi (Professor Radiation Oncology, Dep Book 2010 Springer-Verlag Paris 2010 breast cancer.ca
描述.Why a book dedicated to rare cancer management?. .Given the large variety of rare cancers,they take up a significant part of our daily practice. Therefore, we owe it to our patients with rare tumours that we use the knowledge gained in the treatment of the more common cancers to provide them with a better future. This knowledge comes from recent developments in molecular diagnostics, systemic treatments with new drugs and targeted therapies together with advanced technologies in the areas of radiology and radiation therapy. Our authors have analysed the literature and recommend treatments for rare cancers based on results from past studies. We hope that this book will be an aid to those treating rare cancer cases about which, up to now, little has been published, and will reassure our patients that they have not been forgotten..
出版日期Book 2010
關鍵詞breast cancer; cancer; carcinoma; cell; diagnostics; hematology; lymphoma; oncology; ovarian cancer; radiatio
版次1
doihttps://doi.org/10.1007/978-2-287-92246-6
isbn_softcover978-2-287-92245-9
isbn_ebook978-2-287-92246-6
copyrightSpringer-Verlag Paris 2010
The information of publication is updating

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發(fā)表于 2025-3-21 21:45:44 | 只看該作者
Atypical and malignant meningiomasey Cushing. The arachnoidal origin of this type of tumour was also described at that time. By 1938, Cushing and Eisenhardt had already reported unusually aggressive, brain-invading meningiomas and had classified them as malignant [.]. The incidence of meningioma is approximately 6 per 100,000 [.]. T
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Chordoma and chondrosarcoma of the skull baseprimary malignant bone tumours [.]. The median age at presentation is around 60 years; however, presentation with skull base tumours may occur at a younger age and has been reported in children and adolescents [.]. Chordomas arise from embryonic remains of notochord and show a dual epithelial-mesenc
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Extranodal NK/T-cell lymphoma, nasal-type (REAL)/World Health Organization (WHO) classification of lymphoid tissue [., .]. Clinically, this entity is characterized by a predominance in males, young age of onset, a large proportion of early stage diseases, frequent systematic symptoms, good performance, low-risk international prognostic ind
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Uncomon tumours of the nasopharynxntion is difficult because of the anatomic localisation. For these cases, radiotherapy is preferred as a treatment option due to surgical difficulty. With that scope, treatment options of nasopharyngeal carcinomas, plasmacytomas, angiofibromas, and minor salivary gland tumours will be discussed.
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